A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624766



Internal ID7011616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122096470..122097095hg38UCSC Ensembl
Innerchr10:122096508..122097057hg38UCSC Ensembl
Outerchr10:122096432..122097133hg38UCSC Ensembl
chr10:123855985..123856610hg19UCSC Ensembl
Innerchr10:123856023..123856572hg19UCSC Ensembl
Outerchr10:123855947..123856648hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13953899, essv13953893, essv13953897, essv13953892, essv13953898, essv13953894, essv13953896, essv13953895
SamplesNA19020, HG02090, NA19391, NA19435, NA19310, NA20797, NA19117, HG03439
Known GenesTACC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624766
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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