A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148680



Internal ID15880400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95291631..95362875hg38UCSC Ensembl
Innerchr13:95943885..96015129hg19UCSC Ensembl
Innerchr13:94741886..94813130hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3871245
hg1971245
hg1871245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562772
Supporting Variants
SamplesNINDS_205
Known GenesABCC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148680
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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