A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613950



Internal ID16054673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27746787..28342181hg38UCSC Ensembl
Innerchr9:27746785..28342179hg19UCSC Ensembl
Innerchr9:27736785..28332179hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38595395
hg19595395
hg18595395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132074
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613950
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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