A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2676105

Internal ID9595524
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8245941..8246078hg38UCSC Ensembl
chr17:8149259..8149396hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5733075, essv6160660, essv6495962, essv6164858, essv6214015, essv5687514, essv6425865, essv5655840, essv5879716, essv5469344, essv5420994, essv6561901, essv5958131, essv6389863, essv5744519, essv6475112, essv5722371, essv6555096, essv6569618, essv6529877, essv5990410, essv6128023, essv5404294, essv6158266, essv5853962, essv6260891, essv6439906, essv6397176, essv6152653, essv6529212, essv6169847, essv5477111, essv5456936, essv6355528, essv5797482, essv6053922, essv6160325, essv5658435, essv6151543, essv6130010, essv5577646, essv6061258, essv6355878, essv5951224, essv5818990, essv6289225, essv6377525, essv5576608, essv6214031, essv6021532, essv5703576, essv6330872, essv5805090, essv6330824, essv5483568, essv5853620, essv6154432, essv6288025, essv5775476, essv5515695, essv5437501, essv6023596, essv6126186, essv5779585, essv5517115, essv5564536, essv5993134, essv5513841, essv6471085, essv5885065, essv5959440, essv6521055, essv6524249, essv6434163, essv5716378
SamplesHG00613, NA19312, HG00537, HG00536, HG00607, NA18595, HG00619, HG01250, NA18530, HG00705, HG00437, HG01173, NA18612, HG00449, HG01079, HG01389, HG00657, HG00428, HG00475, HG00375, HG01350, NA18546, NA19379, HG00683, HG00581, HG00651, HG00557, NA19355, HG00253, HG00699, HG00543, NA18559, NA18624, HG00421, HG00583, NA18566, HG00692, HG00689, HG01124, NA18638, HG00419, NA18637, HG00584, NA19377, NA19786, NA18620, HG00653, HG00268, NA19375, HG00501, HG00232, HG01356, HG00524, HG00512, HG00525, NA18562, HG01060, NA18579, HG00589, NA18597, NA18599, HG00650, HG00580, HG00448, NA18577, HG00656, HG01366, HG00422, NA19371, HG00693, NA18549, HG00684, HG00336, HG00702, HG01067
Known GenesCTC1
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2676105
Sample Size1151
Observed Gain0
Observed Loss75
Observed Complex0

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