A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816814



Internal ID16110770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88837014..88912396hg38UCSC Ensembl
Innerchr13:89489268..89564650hg19UCSC Ensembl
Innerchr13:88287269..88362651hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3875383
hg1975383
hg1875383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562636
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)nssv816814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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