A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622103



Internal ID6662273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1514571..1515004hg38UCSC Ensembl
Innerchr10:1514575..1515000hg38UCSC Ensembl
Outerchr10:1514567..1515008hg38UCSC Ensembl
chr10:1556766..1557199hg19UCSC Ensembl
Innerchr10:1556770..1557195hg19UCSC Ensembl
Outerchr10:1556762..1557203hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13665672, essv13665665, essv13665678, essv13665671, essv13665677, essv13665663, essv13665667, essv13665661, essv13665675, essv13665676, essv13665669, essv13665664, essv13665673, essv13665666, essv13665674, essv13665662, essv13665670, essv13665668
SamplesHG01813, HG02165, HG01944, HG01597, HG02397, HG02142, NA18641, HG02028, HG01596, HG02131, HG01872, NA20850, HG02035, HG00530, HG02187, HG02136, NA18549, HG01857
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622103
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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