A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613694



Internal ID16054417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17236378..17377631hg38UCSC Ensembl
Innerchr9:17236376..17377629hg19UCSC Ensembl
Innerchr9:17226376..17367629hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38141254
hg19141254
hg18141254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156258
Samples1780862312_A
Known GenesCNTLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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