A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516500



Internal ID15097107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33434933..33466861hg38UCSC Ensembl
Innerchr9:33434931..33466859hg19UCSC Ensembl
Innerchr9:33424931..33456859hg18UCSC Ensembl
Innerchr9:33424931..33456859hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3831929
hg1931929
hg1831929
hg1731929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682721, nssv668695
Samples
Known GenesAQP3, NOL6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516500
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer