A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1130787



Internal ID15983973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19470633..19533874hg38UCSC Ensembl
Innerchr9:19470631..19533872hg19UCSC Ensembl
Innerchr9:19460631..19523872hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3863242
hg1963242
hg1863242
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613734
Supporting Variants
Samples
Known GenesSLC24A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1130787
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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