A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524317



Internal ID15451610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:90264186..90371181hg38UCSC Ensembl
Innerchr1:90729744..90836739hg19UCSC Ensembl
Innerchr1:90502332..90609327hg18UCSC Ensembl
Innerchr1:90441765..90548760hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38106996
hg19106996
hg18106996
hg17106996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700219
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524317
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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