A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617743



Internal ID7004628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78906631..78915365hg38UCSC Ensembl
Innerchr8:78906631..78915365hg38UCSC Ensembl
Outerchr8:78906131..78915865hg38UCSC Ensembl
chr8:79818866..79827600hg19UCSC Ensembl
Innerchr8:79818866..79827600hg19UCSC Ensembl
Outerchr8:79818366..79828100hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg388735
hg198735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13237766, essv13237767
SamplesNA19347, NA19376
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617743
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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