A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613698



Internal ID16054421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17457856..17488113hg38UCSC Ensembl
Innerchr9:17457854..17488111hg19UCSC Ensembl
Innerchr9:17447854..17478111hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3830258
hg1930258
hg1830258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129325, nssv1129326
Samples
Known GenesCNTLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613698
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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