A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522489



Internal ID15103096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:204396621..204401286hg38UCSC Ensembl
Innerchr1:204365749..204370414hg19UCSC Ensembl
Innerchr1:202632372..202637037hg18UCSC Ensembl
Innerchr1:201097406..201102071hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg384666
hg194666
hg184666
hg174666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705856
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522489
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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