A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817583



Internal ID15764853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97433159..97434472hg38UCSC Ensembl
Innerchr13:98085413..98086726hg19UCSC Ensembl
Innerchr13:96883414..96884727hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381314
hg191314
hg181314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562800
Supporting Variants
Samples
Known GenesRAP2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817583
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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