A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692925



Internal ID15429577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114091517..114104774hg38UCSC Ensembl
Innerchr9:116853797..116867054hg19UCSC Ensembl
Innerchr9:115893618..115906875hg18UCSC Ensembl
Innerchr9:113933351..113946608hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3813258
hg1913258
hg1813258
hg1713258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515856
Supporting Variants
Samples
Known GenesKIF12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692925
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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