A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816598



Internal ID16110554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83572908..83618979hg38UCSC Ensembl
Innerchr13:84147043..84193114hg19UCSC Ensembl
Innerchr13:83045044..83091115hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3846072
hg1946072
hg1846072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562547
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv816598
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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