A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv565e199



Internal ID20123867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73373835..73374703hg38UCSC Ensembl
chr17:71369974..71370842hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38869
hg19869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666306, esv2678522
SamplesNA19137, NA12827, NA18621, NA19207, NA18870, NA18964, NA19248, NA19152, HG00537, NA18861, NA18605, HG00607, NA19712, NA12748, NA18520, NA18595, NA19904, NA18951, NA18534, NA18530, NA18871, HG00418, HG00705, NA18874, HG00437, HG00500, HG01173, HG00369, HG01083, NA18501, NA19093, NA19783, NA19401, HG00565, NA18526, HG00449, NA19060, NA19469, NA19003, NA19072, NA18511, NA19455, NA18603, HG01389, NA20296, NA20775, HG00463, NA18516, NA19359, HG00614, HG01492, NA19453, NA18953, HG01488, NA12828, NA19010, NA19449, NA18542, HG00553, NA18541, NA18546, NA19379, HG00701, HG01167, NA18507, NA19834, HG00581, HG01204, NA18963, NA19004, NA19678, HG01101, NA19474, NA19084, HG00699, NA19472, NA18873, NA18950, NA19761, HG00479, NA18949, NA19438, NA18868, NA19654, NA18632, HG00592, HG00635, NA19077, NA18559, NA19062, NA19463, NA19067, NA18912, NA19383, NA19982, NA19085, NA18624, HG01140, NA18508, NA18967, NA19239, NA19059, HG00593, HG00472, NA19390, HG00421, NA18635, NA19057, NA19675, NA19443, NA19107, NA19722, NA20783, HG00692, NA20807, NA18592, NA18856, NA19398, HG00419, HG00125, NA19835, NA18916, HG00174, HG00637, NA18593, NA19681, NA18634, NA19082, HG00662, NA18539, NA19055, HG00436, NA19080, NA19153, HG00124, HG01465, NA19172, NA19189, NA19372, NA20826, NA18486, NA19102, HG00559, NA06986, NA19238, NA18502, NA19657, NA19713, HG01073, NA18977, NA19098, NA19901, NA18504, NA19704, NA18487, NA18564, NA18942, NA18961, NA19347, NA19909, HG00740, NA18613, HG00534, HG01070, HG00525, NA18562, NA19074, NA19131, NA18910, NA19382, NA19711, NA18974, NA18985, NA19789, NA19462, HG00589, NA18582, HG00427, HG01190, NA19138, HG00443, NA18599, NA18907, NA18909, NA19723, NA19078, NA19201, HG00650, NA18538, NA18565, NA19009, HG00663, NA18989, HG00580, NA19434, HG00608, NA18577, NA19446, NA20509, NA18548, NA19064, NA19160, NA18499, NA18571, NA19371, NA19916, HG01108, NA19070, NA19470, NA18984, HG00566, HG01125, NA19171, NA19240, NA19346, HG00690, NA18549, NA18574, NA19204, HG00442, HG00473, NA19350, NA18908, NA19079, NA20806, HG00626, HG00684, HG00476, NA19448, HG00671, NA18555, NA19385, NA18519, NA19065, HG00126, NA07000, NA19058, HG00531, NA19439, HG00361, HG01198
Known GenesSDK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv565e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss241
Observed Complex0
Frequencyn/a


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