A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636648



Internal ID7023442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59780834..59811789hg38UCSC Ensembl
Innerchr15:59781334..59811289hg38UCSC Ensembl
Outerchr15:59779834..59812789hg38UCSC Ensembl
chr15:60073033..60103988hg19UCSC Ensembl
Innerchr15:60073533..60103488hg19UCSC Ensembl
Outerchr15:60072033..60104988hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3830956
hg1930956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261111, essv15261115, essv15261112, essv15261113, essv15261117, essv15261116, essv15261114, essv15261110
SamplesHG00189, HG01348, HG01051, HG02146, HG00148, HG00365, HG02601, HG02286
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636648
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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