A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141275



Internal ID15647775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114323095..114325784hg38UCSC Ensembl
Innerchr9:117085375..117088064hg19UCSC Ensembl
Innerchr9:116125196..116127885hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382690
hg192690
hg182690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615246
Supporting Variants
Samples
Known GenesORM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141275
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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