A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520782



Internal ID15448075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:170816429..171173879hg38UCSC Ensembl
Innerchr5:170243433..170600883hg19UCSC Ensembl
Innerchr5:170176011..170533488hg18UCSC Ensembl
Innerchr5:170176011..170533488hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38357451
hg19357451
hg18357478
hg17357478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697606
Samples
Known GenesRANBP17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520782
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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