A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613933



Internal ID16401342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26265881..26417860hg38UCSC Ensembl
Innerchr9:26265879..26417858hg19UCSC Ensembl
Innerchr9:26255879..26407858hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38151980
hg19151980
hg18151980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12618n54
Supporting Variantsnssv1132062, nssv1132065, nssv1132064, nssv1132063
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613933
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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