A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816732



Internal ID16110688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86540492..87275195hg38UCSC Ensembl
Innerchr13:87192747..87927450hg19UCSC Ensembl
Innerchr13:85990748..86725451hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38734704
hg19734704
hg18734704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562621
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)nssv816732
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