A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613433



Internal ID16054156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11606348..11716862hg38UCSC Ensembl
Innerchr9:11606348..11716862hg19UCSC Ensembl
Innerchr9:11596348..11706862hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38110515
hg19110515
hg18110515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128553
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613433
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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