A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13856343



Internal ID6429296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69683592..69689532hg38UCSC Ensembl
Innerchr10:69683601..69689524hg38UCSC Ensembl
Outerchr10:69683584..69689541hg38UCSC Ensembl
chr10:71443348..71449288hg19UCSC Ensembl
Innerchr10:71443357..71449280hg19UCSC Ensembl
Outerchr10:71443340..71449297hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385941
hg195941
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623752
Supporting Variants
SamplesNA20505
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13856343
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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