A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816278



Internal ID16110234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:82593242..82609577hg38UCSC Ensembl
Innerchr13:83167377..83183712hg19UCSC Ensembl
Innerchr13:82065378..82081713hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3816336
hg1916336
hg1816336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562496
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)nssv816278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer