A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518455



Internal ID294844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32494921..32494975hg38UCSC Ensembl
chr20:31082724..31082778hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731957
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518455
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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