A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616159



Internal ID6656356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8931170..8932877hg38UCSC Ensembl
Innerchr8:8931203..8932845hg38UCSC Ensembl
Outerchr8:8931138..8932910hg38UCSC Ensembl
chr8:8788680..8790387hg19UCSC Ensembl
Innerchr8:8788713..8790355hg19UCSC Ensembl
Outerchr8:8788648..8790420hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381708
hg191708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13093744, essv13093743
SamplesNA20761, HG01684
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616159
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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