A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732514



Internal ID156180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43847612..43852107hg38UCSC Ensembl
chr20:42476252..42480747hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg384496
hg194496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523765
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732514
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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