A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518296



Internal ID15098903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62203245..62415019hg38UCSC Ensembl
Innerchr20:60778301..60990075hg19UCSC Ensembl
Innerchr20:60211696..60423470hg18UCSC Ensembl
Innerchr20:60211696..60423470hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38211775
hg19211775
hg18211775
hg17211775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695727
Samples
Known GenesADRM1, CABLES2, HRH3, LAMA5, MIR4758, OSBPL2, RBBP8NL, RPS21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518296
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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