A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613969



Internal ID16401378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28202094..28340973hg38UCSC Ensembl
Innerchr9:28202092..28340971hg19UCSC Ensembl
Innerchr9:28192092..28330971hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38138880
hg19138880
hg18138880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12625n54
Supporting Variantsnssv1132112
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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