A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733250



Internal ID156916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56681657..56685566hg38UCSC Ensembl
chr20:55256713..55260622hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg383910
hg193910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733250
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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