A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517374



Internal ID15444667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129867142..129878447hg38UCSC Ensembl
Innerchr9:132629421..132640726hg19UCSC Ensembl
Innerchr9:131669242..131680547hg18UCSC Ensembl
Innerchr9:129708975..129720280hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3811306
hg1911306
hg1811306
hg1711306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679484, nssv653886
Samples
Known GenesMIR6855, USP20
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517374
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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