A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527274



Internal ID15454567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17638179..17650928hg38UCSC Ensembl
Innerchr20:17618824..17631573hg19UCSC Ensembl
Innerchr20:17566824..17579573hg18UCSC Ensembl
Innerchr20:17566824..17579573hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3812750
hg1912750
hg1812750
hg1712750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703684
Samples
Known GenesRRBP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527274
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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