A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615926



Internal ID16056649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135711894..135789055hg38UCSC Ensembl
Innerchr9:138603740..138680901hg19UCSC Ensembl
Innerchr9:137743561..137820722hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3877162
hg1977162
hg1877162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12994n54
Supporting Variantsnssv1148253
Samples
Known GenesKCNT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615926
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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