A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519680



Internal ID15100287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2882833..2885330hg38UCSC Ensembl
Innerchr20:2863479..2865976hg19UCSC Ensembl
Innerchr20:2811479..2813976hg18UCSC Ensembl
Innerchr20:2811479..2813976hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382498
hg192498
hg182498
hg172498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696989
Samples
Known GenesPTPRA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519680
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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