A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613970



Internal ID16401379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28202094..28342181hg38UCSC Ensembl
Innerchr9:28202092..28342179hg19UCSC Ensembl
Innerchr9:28192092..28332179hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38140088
hg19140088
hg18140088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12625n54
Supporting Variantsnssv1132114, nssv1132113
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613970
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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