A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568785



Internal ID16009508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31325910..31328582hg38UCSC Ensembl
Innerchr15:31618113..31620785hg19UCSC Ensembl
Innerchr15:29405405..29408077hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382673
hg192673
hg182673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4432n54
Supporting Variantsnssv839546, nssv839545, nssv839547, nssv839544
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568785
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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