A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817582



Internal ID15764852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97433146..97434574hg38UCSC Ensembl
Innerchr13:98085400..98086828hg19UCSC Ensembl
Innerchr13:96883401..96884829hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381429
hg191429
hg181429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562799
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)nssv817582
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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