A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732835



Internal ID156501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49568386..49568452hg38UCSC Ensembl
chr20:48184923..48184989hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732835
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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