A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816569



Internal ID16110525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83528305..83591492hg38UCSC Ensembl
Innerchr13:84102440..84165627hg19UCSC Ensembl
Innerchr13:83000441..83063628hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3863188
hg1963188
hg1863188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562534
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)nssv816569
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