A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663062



Internal ID9582481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155802622..155815928hg38UCSC Ensembl
Outerchr7:155802251..155816298hg38UCSC Ensembl
Innerchr7:155595316..155608622hg19UCSC Ensembl
Outerchr7:155594945..155608992hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3814048
hg1914048
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
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663062
Frequency
Sample Size1151
Observed Gain0
Observed Loss52
Observed Complex0
Frequencyn/a


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