A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670645



Internal ID9936750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39766904..39767210hg38UCSC Ensembl
chr19:40257544..40257850hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5914797, essv6299225, essv6580971, essv6350693, essv6160002, essv5663081, essv5601970, essv5622733, essv6495966, essv6534491, essv5818740, essv5848320, essv5676242, essv6121260, essv5894704, essv6241760, essv5879703, essv6099197, essv6057159, essv6408510, essv6034386, essv6387700, essv6399888, essv5693146, essv6321191, essv5629468, essv6407103, essv6533445, essv6381853, essv5557383, essv6317047, essv6298396, essv5794493, essv5997233, essv6154412, essv5676990, essv6405567, essv6067186, essv6495421, essv6353820, essv5477232, essv6036704, essv6163748, essv5994314, essv5455350, essv6017945, essv6239486, essv5627950, essv6368132, essv5933197, essv6504466, essv5607694, essv6595756, essv5940429, essv5906788, essv5568167, essv6069663, essv6293450, essv5733022, essv6216224, essv6233190, essv5673166, essv5557824, essv5638477, essv6532602, essv5849123, essv5732720, essv5482440, essv5795765, essv5793369, essv6309733, essv6203210, essv5426364, essv6397079, essv6250850, essv5970538, essv5718161, essv5895483, essv6338161, essv5711066, essv5819277, essv5953781, essv5754504, essv6507865, essv5896577, essv6180723, essv6489171, essv6255651, essv6413574, essv5908109, essv5847578, essv6525040, essv6581700, essv5453624, essv5568918, essv6586558, essv6051216, essv5666461, essv6179371, essv6299229, essv5464460, essv5661647, essv6425874, essv6538217, essv5897833, essv6132483, essv5944589, essv6318979, essv6443359, essv5457405, essv6202382, essv5788914, essv5658806, essv6123378, essv5660439, essv5675378, essv5403252, essv6524376, essv5821513, essv5528454, essv6329312, essv5473677, essv6030715, essv6297722, essv5463714, essv6138932, essv6239037, essv6123892, essv6369948, essv6148488, essv6332527, essv5567238, essv6293522, essv6433506, essv6484325, essv6310340, essv6068903, essv6348063, essv6370691, essv5915955, essv5604088, essv5976859, essv6403120, essv5752099, essv5768432, essv6353974, essv5662453, essv5865482, essv6146107, essv6044598, essv6009793, essv6277892, essv6345222, essv6138535, essv5527591, essv6086502, essv6422029, essv6092106, essv6358736, essv6311829, essv5912586, essv6497976, essv5464953, essv6367919, essv6485454, essv6575400, essv6297217, essv6189851, essv6442122, essv6128761, essv6387529, essv6230748, essv5663310, essv6440965, essv5422472, essv6469004, essv5624723, essv6403023, essv6420621, essv5751511, essv5599897, essv6243213, essv5734238, essv5574134, essv5487756, essv5439618, essv6538623, essv6015789, essv5735708, essv5535706, essv5993445, essv6477894, essv6511528, essv6327017, essv5458117, essv5462828, essv5972467, essv6426615, essv5424900, essv6302793, essv6086133, essv5695897, essv5719744, essv6397544, essv6551304, essv5930322, essv6517302, essv5887287, essv6264613, essv5730137, essv6271465, essv5690745, essv6003319, essv6273097, essv5605626, essv5910991, essv5466644, essv5618510, essv6398230, essv5823189, essv5889046, essv5986826, essv6264580, essv6220075, essv6216439, essv5415767, essv5759188, essv5594227, essv6107985, essv6315011, essv6312631
SamplesNA19394, NA18502, HG00650, HG00542, NA12717, HG00143, NA18621, NA12286, HG00242, NA19204, NA18861, NA19399, NA11920, HG01066, NA18999, HG00244, NA19350, NA12751, NA18504, NA19377, NA18530, NA18959, NA18616, HG00654, HG00261, NA18510, NA12750, HG00693, NA18988, NA12813, HG00663, NA20814, NA18563, NA19171, NA18940, NA18597, NA19678, NA20756, NA18567, NA20795, NA07347, NA19457, NA18571, NA11930, HG00512, NA20759, NA19720, HG00232, NA19238, NA12044, NA11994, NA19207, NA19172, NA18557, HG00323, NA19921, NA18951, NA20800, HG00245, NA18933, NA20760, NA19455, NA19663, HG00344, NA18572, NA18948, HG00551, NA18981, NA18548, NA18573, HG00250, NA20581, HG00331, NA19453, NA18532, NA06989, NA19059, NA19452, HG00463, NA19469, NA12778, HG00246, NA18570, NA19625, NA18593, HG01107, HG01075, NA18974, NA18953, HG00258, NA18632, HG00254, NA19390, HG00336, NA18517, HG00625, NA18628, NA20815, HG01357, HG01174, NA20530, NA19679, NA20544, NA18943, NA12763, NA18615, NA12347, HG00614, NA06994, HG00478, NA20786, NA18873, NA20758, HG00274, NA18989, NA18968, NA18623, NA19065, HG00403, NA19648, NA11830, HG01356, NA11829, NA18592, HG00187, HG01079, NA20531, NA18599, HG01389, NA18603, NA12045, NA18486, HG00103, NA18606, HG00177, NA19190, NA19098, NA12400, NA18967, NA19005, NA18550, NA19201, NA18489, NA18595, HG00689, NA19723, NA19119, NA18982, NA18619, NA19131, NA18942, HG00369, NA18498, NA19782, NA20541, NA12761, NA19137, NA18617, NA18986, NA19159, NA19901, NA19209, NA12828, NA18975, NA20533, NA19451, NA19200, HG00264, HG00260, HG00543, NA18544, NA19210, NA19082, NA20524, NA19077, NA19152, HG00701, NA19391, HG00320, HG00533, HG00500, NA18910, NA18976, NA20770, NA18566, HG01094, NA19000, NA19655, HG01197, NA12892, HG00613, NA18853, NA19338, NA19257, NA19225, NA20828, NA19160, NA20542, NA18634, NA19436, NA20765, HG00124, NA20522, NA18542, NA12716, NA18909, NA18535, NA18961, NA12775, NA19473, NA19435, NA19144, NA07051, HG00607, NA20504, NA06986, HG00269, HG00111, NA18971, NA19438, HG00656, NA18972, HG00252, HG00472, NA19004, NA18511, HG00180, NA18622, HG00437, NA19153, NA18562
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670645
Frequency
Sample Size1151
Observed Gain0
Observed Loss231
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer