A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613987



Internal ID16054710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28570654..28892213hg38UCSC Ensembl
Innerchr9:28570652..28892211hg19UCSC Ensembl
Innerchr9:28560652..28882211hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38321560
hg19321560
hg18321560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12628n54
Supporting Variantsnssv1132130
Samples
Known GenesLINGO2, MIR873, MIR876
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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