A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839539



Internal ID15786809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31325910..31328232hg38UCSC Ensembl
Innerchr15:31618113..31620435hg19UCSC Ensembl
Innerchr15:29405405..29407727hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382323
hg192323
hg182323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568784
Supporting Variants
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839539
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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