A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807429



Internal ID16101385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:32957296..32978544hg38UCSC Ensembl
Innerchr13:33531434..33552682hg19UCSC Ensembl
Innerchr13:32429434..32450682hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3821249
hg1921249
hg1821249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561434
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)nssv807429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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