A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515856



Internal ID15442913
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692925, nssv701100, nssv665029
Samples
Known GenesKIF12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515856
Frequency
Sample Size2026
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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