A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv818822



Internal ID16112778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103032716..103048516hg38UCSC Ensembl
Innerchr13:103685066..103700866hg19UCSC Ensembl
Innerchr13:102483067..102498867hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3815801
hg1915801
hg1815801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562982
Supporting Variants
Samples
Known GenesSLC10A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv818822
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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