A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677427



Internal ID9943532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168295960..168296170hg38UCSC Ensembl
chr6:168696640..168696850hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6366449, essv6271793, essv6390843, essv5646539, essv5893519, essv5885880, essv5516030, essv6577974, essv5794057, essv6352330, essv5674037, essv6065278, essv5413928, essv5876340, essv5609822, essv5476210, essv5780594, essv6041156, essv6597783, essv5790723, essv5932009, essv6206084, essv6162290, essv6478336, essv6582945, essv6314648, essv5908935, essv5502348, essv6199308, essv6234651, essv6405707, essv5491364, essv5668985, essv5982778, essv5820780, essv5717935, essv5645678, essv6089884, essv5638060, essv5919017, essv6559739, essv5922272, essv6330774, essv6597591, essv5895239, essv5735599, essv6501800, essv6139223, essv5658142, essv6386196, essv6094908, essv5505563, essv5550909, essv5713484, essv6235951, essv5733323, essv5612462, essv6428684, essv6382969, essv5751405, essv5432967, essv6028655, essv6593079, essv5461897, essv5421167, essv5507666, essv6362158, essv6441256, essv6594808, essv6570073, essv5865799, essv6187835, essv6199874, essv5435365, essv5547166, essv5584025, essv5889536, essv5493774, essv6178509, essv6044532, essv5633915, essv6568880, essv6468639, essv5560382, essv6103792, essv5889422, essv5645446, essv6283239, essv5805895, essv6063938, essv6319656, essv6328047, essv6569921, essv6288125, essv6417640, essv5453880, essv5820586, essv6112781, essv5687097, essv5486314, essv5952029, essv6162384, essv5833919, essv6587956, essv6218335, essv6241799, essv6065558, essv5419065, essv5867316, essv5601048, essv5844744
SamplesHG00626, NA19394, HG00442, NA12842, NA19397, HG00608, HG00671, HG00559, HG01079, HG01389, HG01374, NA19355, NA18530, NA18606, HG00654, HG00693, HG00327, HG00663, NA19374, HG01250, NA19396, NA19381, NA18944, NA18550, HG01070, HG00589, NA18597, NA18595, HG00702, HG00448, NA18635, NA18558, HG00634, NA18942, NA18582, NA19457, HG01083, NA19138, HG00334, HG00590, NA18611, HG00512, HG01069, HG01067, HG01519, HG01170, NA18977, HG00534, HG00422, NA19087, HG01440, HG00427, HG01048, HG00326, HG00530, HG00543, HG00313, NA18544, NA18613, NA18933, HG00653, HG00657, HG00475, HG00556, HG00584, HG00533, HG00583, NA18637, HG00500, HG00275, NA18572, HG00619, HG00708, HG00692, HG00740, HG01390, HG01047, NA18566, HG00651, HG00690, HG00479, HG00331, HG00704, HG00463, NA19401, NA18632, NA19390, HG00285, NA18543, NA18559, NA19434, NA19072, HG01357, HG01174, NA19428, NA19083, NA19328, HG00672, HG00614, HG00513, NA20348, HG00186, HG00698, HG00345, NA18549, NA18622, HG00437, NA18562, HG00581, NA18577, HG00593
Known GenesDACT2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677427
Frequency
Sample Size1151
Observed Gain0
Observed Loss111
Observed Complex0
Frequencyn/a


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