A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696989



Internal ID15086955
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519680
Supporting Variants
Samples
Known GenesPTPRA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696989
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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