A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10989677



Internal ID2787660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41028406..41029299hg38UCSC Ensembl
Innerchr3:41028419..41029287hg38UCSC Ensembl
Outerchr3:41028394..41029312hg38UCSC Ensembl
chr3:41069897..41070790hg19UCSC Ensembl
Innerchr3:41069910..41070778hg19UCSC Ensembl
Outerchr3:41069885..41070803hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595963
Supporting Variants
SamplesHG02462
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10989677
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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