A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817663



Internal ID16111619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97871212..97879858hg38UCSC Ensembl
Innerchr13:98523466..98532112hg19UCSC Ensembl
Innerchr13:97321467..97330113hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg388647
hg198647
hg188647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562825
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)nssv817663
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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