A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613696



Internal ID16054419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17329966..17438393hg38UCSC Ensembl
Innerchr9:17329964..17438391hg19UCSC Ensembl
Innerchr9:17319964..17428391hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38108428
hg19108428
hg18108428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129324
Samples
Known GenesCNTLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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