A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568786



Internal ID16009509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31325910..31329118hg38UCSC Ensembl
Innerchr15:31618113..31621321hg19UCSC Ensembl
Innerchr15:29405405..29408613hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383209
hg193209
hg183209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4432n54
Supporting Variantsnssv839548
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568786
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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