A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705496



Internal ID15442148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114053497..114104774hg38UCSC Ensembl
Innerchr9:116815777..116867054hg19UCSC Ensembl
Innerchr9:115855598..115906875hg18UCSC Ensembl
Innerchr9:113895331..113946608hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3851278
hg1951278
hg1851278
hg1751278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528822
Supporting Variants
Samples
Known GenesAMBP, KIF12, ZNF618
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705496
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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