A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731476



Internal ID155142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20496117..20496178hg38UCSC Ensembl
chr20:20476761..20476822hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518291
Supporting Variants
Samples
Known GenesRALGAPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731476
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.010615


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