A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519114



Internal ID15446407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:167034302..167045947hg38UCSC Ensembl
Innerchr1:167003539..167015184hg19UCSC Ensembl
Innerchr1:165270163..165281808hg18UCSC Ensembl
Innerchr1:163735197..163746842hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3811646
hg1911646
hg1811646
hg1711646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696590
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519114
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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