A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615066



Internal ID16402475
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 StatusM
Merged Variants
Supporting Variantsnssv1140804
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615066
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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