A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526836



Internal ID15107443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3342549..3342619hg38UCSC Ensembl
Innerchr1:3259113..3259183hg19UCSC Ensembl
Innerchr1:3248973..3249043hg18UCSC Ensembl
Innerchr1:3282270..3282340hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3871
hg1971
hg1871
hg1771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703193
Samples
Known GenesPRDM16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526836
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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