A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732878



Internal ID156544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50326855..50330067hg38UCSC Ensembl
chr20:48943392..48946604hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg383213
hg193213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732878
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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