A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568795



Internal ID16009518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31326320..31328582hg38UCSC Ensembl
Innerchr15:31618523..31620785hg19UCSC Ensembl
Innerchr15:29405815..29408077hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382263
hg192263
hg182263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4432n54
Supporting Variantsnssv839572
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568795
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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