A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616704



Internal ID6656900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26737549..26747280hg38UCSC Ensembl
Innerchr8:26737582..26747248hg38UCSC Ensembl
Outerchr8:26737517..26747313hg38UCSC Ensembl
chr8:26595066..26604797hg19UCSC Ensembl
Innerchr8:26595099..26604765hg19UCSC Ensembl
Outerchr8:26595034..26604830hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg389732
hg199732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13149677
SamplesHG01396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616704
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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