A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568778



Internal ID16009501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31325674..31328083hg38UCSC Ensembl
Innerchr15:31617877..31620286hg19UCSC Ensembl
Innerchr15:29405169..29407578hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382410
hg192410
hg182410
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4431n54
Supporting Variantsnssv839511, nssv839515, nssv839512, nssv839514, nssv839513
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568778
Frequency
Sample Size17421
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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