A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2663062

Internal ID9582481
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155802622..155815928hg38UCSC Ensembl
Outerchr7:155802251..155816298hg38UCSC Ensembl
Innerchr7:155595316..155608622hg19UCSC Ensembl
Outerchr7:155594945..155608992hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5781028, essv5979289, essv6496444, essv5851131, essv6477702, essv6489126, essv5844632, essv5580872, essv5710063, essv6026214, essv6027336, essv5943960, essv5494377, essv5576785, essv5899722, essv6291431, essv5660241, essv5400478, essv5511052, essv6584788, essv5523287, essv6095056, essv5566249, essv6016565, essv5788685, essv5493244, essv5860235, essv6155638, essv6505792, essv6069215, essv5740812, essv5588729, essv5506176, essv6386713, essv5402442, essv6204521, essv5927792, essv6019480, essv6459515, essv6205181, essv6311257, essv5868466, essv5514690, essv6261530, essv6586369, essv5941723, essv5530479, essv5660014, essv5397101, essv5906910, essv6533217, essv6070138
SamplesHG00613, HG00537, HG00536, HG00418, HG00500, HG00596, HG00449, HG00707, HG00428, HG00475, HG00542, HG00701, HG00683, HG00698, HG00404, HG00651, HG00578, HG00699, HG00543, HG00556, HG00472, HG00421, HG00583, HG00610, HG00689, HG00533, HG00419, HG00634, HG00403, HG00620, HG00629, HG00501, HG00672, HG00513, HG00512, HG00534, HG00525, HG00427, HG00595, HG00611, HG00650, HG00448, HG00654, HG00530, HG00656, HG00422, HG00708, HG00625, HG00690, HG00626, HG00671, HG00531
Known GenesSHH
AnalysisNo reference, merging analysis
CommentsHigh quality site
Pubmed ID23128226
Accession Number(s)esv2663062
Sample Size1151
Observed Gain0
Observed Loss52
Observed Complex0

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