A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139760



Internal ID15646260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98420416..98918098hg38UCSC Ensembl
Innerchr9:101182698..101680380hg19UCSC Ensembl
Innerchr9:100222519..100720201hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38497683
hg19497683
hg18497683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614936
Supporting Variants
Samples
Known GenesANKS6, GABBR2, GALNT12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1139760
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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