A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839563



Internal ID15786833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31326081..31328530hg38UCSC Ensembl
Innerchr15:31618284..31620733hg19UCSC Ensembl
Innerchr15:29405576..29408025hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382450
hg192450
hg182450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568790
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)nssv839563
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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