A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616872



Internal ID7003758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34961825..34966746hg38UCSC Ensembl
Innerchr8:34961839..34966733hg38UCSC Ensembl
Outerchr8:34961812..34966760hg38UCSC Ensembl
chr8:34819343..34824264hg19UCSC Ensembl
Innerchr8:34819357..34824251hg19UCSC Ensembl
Outerchr8:34819330..34824278hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384922
hg194922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13165852
SamplesHG02179
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616872
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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