A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521123



Internal ID15448416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:90305008..90371181hg38UCSC Ensembl
Innerchr1:90770566..90836739hg19UCSC Ensembl
Innerchr1:90543154..90609327hg18UCSC Ensembl
Innerchr1:90482587..90548760hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3866174
hg1966174
hg1866174
hg1766174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697801
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521123
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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