A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701100



Internal ID15437752
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 loss
Copy Number
Allele StateHeterozygous
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)nssv701100
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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