A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13690251



Internal ID3692067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8020040..8026272hg38UCSC Ensembl
Innerchr10:8020040..8026272hg38UCSC Ensembl
Outerchr10:8019953..8026353hg38UCSC Ensembl
chr10:8062003..8068235hg19UCSC Ensembl
Innerchr10:8062003..8068235hg19UCSC Ensembl
Outerchr10:8061916..8068316hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386233
hg196233
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622280
Supporting Variants
SamplesHG00345
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13690251
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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