A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839555



Internal ID15786825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31326081..31328083hg38UCSC Ensembl
Innerchr15:31618284..31620286hg19UCSC Ensembl
Innerchr15:29405576..29407578hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382003
hg192003
hg182003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568788
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)nssv839555
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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