A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140804



Internal ID15993990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104224862..104367119hg38UCSC Ensembl
Innerchr9:106987143..107129400hg19UCSC Ensembl
Innerchr9:106026964..106169221hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38142258
hg19142258
hg18142258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615066
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1140804
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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