A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562345



Internal ID16349754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:74463719..74491648hg38UCSC Ensembl
Innerchr13:75037856..75065785hg19UCSC Ensembl
Innerchr13:73935857..73963786hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3827930
hg1927930
hg1827930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815763
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562345
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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