A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613722



Internal ID16401131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17951333..17970622hg38UCSC Ensembl
Innerchr9:17951331..17970620hg19UCSC Ensembl
Innerchr9:17941331..17960620hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3819290
hg1919290
hg1819290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130779
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613722
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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