A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522391



Internal ID15449684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:43081149..43110650hg38UCSC Ensembl
Innerchr1:43546820..43576321hg19UCSC Ensembl
Innerchr1:43319407..43348908hg18UCSC Ensembl
Innerchr1:43215913..43245414hg17UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3829502
hg1929502
hg1829502
hg1729502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695171
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522391
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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