A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613284



Internal ID16400693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8165192..8279622hg38UCSC Ensembl
Innerchr9:8165192..8279622hg19UCSC Ensembl
Innerchr9:8155192..8269622hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38114431
hg19114431
hg18114431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126879
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613284
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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