A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613946



Internal ID16401355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27179246..27234031hg38UCSC Ensembl
Innerchr9:27179244..27234029hg19UCSC Ensembl
Innerchr9:27169244..27224029hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3854786
hg1954786
hg1854786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132073
Samples
Known GenesTEK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613946
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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