A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662159



Internal ID15052125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112636784..112795966hg38UCSC Ensembl
Innerchr9:115399064..115558246hg19UCSC Ensembl
Innerchr9:114438885..114598067hg18UCSC Ensembl
Innerchr9:112478619..112637801hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38159183
hg19159183
hg18159183
hg17159183
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)nssv662159
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