A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693083



Internal ID15083049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112628168..112795966hg38UCSC Ensembl
Innerchr9:115390448..115558246hg19UCSC Ensembl
Innerchr9:114430269..114598067hg18UCSC Ensembl
Innerchr9:112470003..112637801hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38167799
hg19167799
hg18167799
hg17167799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515899
Supporting Variants
Samples
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693083
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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