A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615435



Internal ID16402844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129431819..129466284hg38UCSC Ensembl
Innerchr9:132194098..132228563hg19UCSC Ensembl
Innerchr9:131233919..131268384hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3834466
hg1934466
hg1834466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12895n54
Supporting Variantsnssv1144786
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615435
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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