A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694299



Internal ID15084265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105609268..105692464hg38UCSC Ensembl
Innerchr9:108371549..108454745hg19UCSC Ensembl
Innerchr9:107411370..107494566hg18UCSC Ensembl
Innerchr9:105451104..105534300hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3883197
hg1983197
hg1883197
hg1783197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519023
Supporting Variants
Samples
Known GenesFKTN, TAL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694299
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