A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176058



Internal ID15855402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63858789..64794358hg38UCSC Ensembl
Innerchr13:64432922..65368490hg19UCSC Ensembl
Innerchr13:63330923..64266491hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38935570
hg19935569
hg18935569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561965
Supporting Variants
Samples1780862585_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176058
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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