A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732559



Internal ID156225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44635941..44635995hg38UCSC Ensembl
chr20:43264582..43264636hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521152
Supporting Variants
Samples
Known GenesADA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732559
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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