A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820683



Internal ID15767953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113755091..113853604hg38UCSC Ensembl
Innerchr13:114458064..114556577hg19UCSC Ensembl
Innerchr13:113557366..113656067hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3898514
hg1998514
hg1898702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563389
Supporting Variants
Samples
Known GenesGAS6, GAS6-AS1, TMEM255B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820683
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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