A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624713



Internal ID7011563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119717775..119722490hg38UCSC Ensembl
Innerchr10:119717793..119722473hg38UCSC Ensembl
Outerchr10:119717758..119722508hg38UCSC Ensembl
chr10:121477287..121482002hg19UCSC Ensembl
Innerchr10:121477305..121481985hg19UCSC Ensembl
Outerchr10:121477270..121482020hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384716
hg194716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13948133, essv13948134, essv13948136, essv13948135, essv13948137
SamplesHG02574, HG02836, HG01893, HG02837, HG02314
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624713
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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