A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817566



Internal ID15764836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96090131..96090785hg38UCSC Ensembl
Innerchr13:96742385..96743039hg19UCSC Ensembl
Innerchr13:95540386..95541040hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38655
hg19655
hg18655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562787
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)nssv817566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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