A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616860



Internal ID7003746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34615006..34615628hg38UCSC Ensembl
Innerchr8:34615009..34615626hg38UCSC Ensembl
Outerchr8:34615004..34615631hg38UCSC Ensembl
chr8:34472524..34473146hg19UCSC Ensembl
Innerchr8:34472527..34473144hg19UCSC Ensembl
Outerchr8:34472522..34473149hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13164638, essv13164643, essv13164641, essv13164639, essv13164640, essv13164642
SamplesNA19315, NA19038, NA19451, NA19401, NA19108, HG02763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616860
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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