A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520925



Internal ID15101532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33021637..33033627hg38UCSC Ensembl
Innerchr21:34393945..34405935hg19UCSC Ensembl
Innerchr21:33315815..33327805hg18UCSC Ensembl
Innerchr21:33315815..33327805hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3811991
hg1911991
hg1811991
hg1711991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677737, nssv682329, nssv687408
Samples
Known GenesOLIG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520925
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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