A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623036



Internal ID7009893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43066764..43073925hg38UCSC Ensembl
Innerchr10:43066774..43073916hg38UCSC Ensembl
Outerchr10:43066755..43073935hg38UCSC Ensembl
chr10:43562212..43569373hg19UCSC Ensembl
Innerchr10:43562222..43569364hg19UCSC Ensembl
Outerchr10:43562203..43569383hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387162
hg197162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764231, essv13764232, essv13764233
SamplesHG00306, NA19792, NA20516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623036
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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