A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731444



Internal ID155110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20032015..20032459hg38UCSC Ensembl
chr20:20012659..20013103hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515004
Supporting Variants
Samples
Known GenesNAA20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.011708


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