A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv809967



Internal ID15757237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:42901055..43222033hg38UCSC Ensembl
Innerchr13:43475191..43796169hg19UCSC Ensembl
Innerchr13:42373191..42694169hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38320979
hg19320979
hg18320979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561565
Supporting Variants
Samples
Known GenesDNAJC15, ENOX1, EPSTI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv809967
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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