A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15270979



Internal ID5638956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63496772..63499450hg38UCSC Ensembl
Innerchr15:63496822..63499400hg38UCSC Ensembl
Outerchr15:63496722..63499500hg38UCSC Ensembl
chr15:63788971..63791649hg19UCSC Ensembl
Innerchr15:63789021..63791599hg19UCSC Ensembl
Outerchr15:63788921..63791699hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382679
hg192679
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636718
Supporting Variants
SamplesNA19062
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15270979
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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