A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132844



Internal ID15986030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33817136..33817674hg38UCSC Ensembl
Innerchr9:33817134..33817672hg19UCSC Ensembl
Innerchr9:33807134..33807672hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38539
hg19539
hg18539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614152
Supporting Variants
Samples
Known GenesUBE2R2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1132844
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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