A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732207



Internal ID155873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36557731..36566540hg38UCSC Ensembl
chr20:35186134..35194943hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg388810
hg198810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732207
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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