A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839564



Internal ID15786834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31326081..31328582hg38UCSC Ensembl
Innerchr15:31618284..31620785hg19UCSC Ensembl
Innerchr15:29405576..29408077hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382502
hg192502
hg182502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568791
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)nssv839564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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