A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562951



Internal ID16350360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99421411..99440877hg38UCSC Ensembl
Innerchr13:100073665..100093131hg19UCSC Ensembl
Innerchr13:98871666..98891132hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3819467
hg1919467
hg1819467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149457
Samples1780854483_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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