A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725949



Internal ID149615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40379912..40381841hg38UCSC Ensembl
chr20:39008552..39010481hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381930
hg191930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725949
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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