A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519722



Internal ID15100329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37239816..37242821hg38UCSC Ensembl
Innerchr20:35868219..35871224hg19UCSC Ensembl
Innerchr20:35301633..35304638hg18UCSC Ensembl
Innerchr20:35301633..35304638hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383006
hg193006
hg183006
hg173006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697012
Samples
Known GenesRPN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519722
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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