A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613052



Internal ID16400461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1311310..1662585hg38UCSC Ensembl
Innerchr9:1311310..1662585hg19UCSC Ensembl
Innerchr9:1301310..1652585hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38351276
hg19351276
hg18351276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126037
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613052
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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