A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663767



Internal ID9929872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99476966..99477266hg38UCSC Ensembl
Outerchr13:99476906..99477345hg38UCSC Ensembl
Innerchr13:100129220..100129520hg19UCSC Ensembl
Outerchr13:100129160..100129599hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5436058, essv5999912, essv5865042, essv6344446, essv6255851, essv6034712, essv5609308, essv5917397, essv5846368, essv6320959, essv6445080, essv6060887, essv5965047, essv6126705, essv6427716, essv6356813, essv5947928, essv6418684, essv6557978, essv5614135, essv6537121, essv6044585, essv6551553, essv6547474, essv5952935, essv6558931, essv6495484, essv6176366, essv5461020, essv5901916, essv5405226, essv6301827, essv5816970, essv5780122, essv6142488, essv5570909, essv5945550, essv5927669, essv5621788, essv5868845
SamplesNA20588, HG00442, HG01462, HG01066, NA19819, NA18596, NA18606, NA07346, NA20796, HG00251, NA19448, HG00346, HG00369, NA18498, NA19130, NA20541, HG00512, NA19372, HG00326, NA20755, HG00543, NA18605, HG00268, NA19707, NA12003, NA19461, HG00651, NA18912, NA12778, HG01075, HG00254, NA19390, HG00278, NA19818, NA19376, HG01055, NA19213, NA18522, HG01437, NA18562
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663767
Frequency
Sample Size1151
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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