A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv815915



Internal ID16109871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80099056..80112015hg38UCSC Ensembl
Innerchr13:80673191..80686150hg19UCSC Ensembl
Innerchr13:79571192..79584151hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3812960
hg1912960
hg1812960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562418
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)nssv815915
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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