A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817759



Internal ID15765029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98142480..98143998hg38UCSC Ensembl
Innerchr13:98794734..98796252hg19UCSC Ensembl
Innerchr13:97592735..97594253hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381519
hg191519
hg181519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562853
Supporting Variants
Samples
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817759
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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