A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636657



Internal ID7023451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60276952..60288441hg38UCSC Ensembl
Innerchr15:60276968..60288425hg38UCSC Ensembl
Outerchr15:60276936..60288457hg38UCSC Ensembl
chr15:60569151..60580640hg19UCSC Ensembl
Innerchr15:60569167..60580624hg19UCSC Ensembl
Outerchr15:60569135..60580656hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3811490
hg1911490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261143
SamplesNA20876
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636657
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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