A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522310



Internal ID15449603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166068238..166223825hg38UCSC Ensembl
Innerchr3:165786026..165941613hg19UCSC Ensembl
Innerchr3:167268720..167424307hg18UCSC Ensembl
Innerchr3:167268728..167424315hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38155588
hg19155588
hg18155588
hg17155588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695090
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522310
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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