A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733223



Internal ID156889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56365907..56366003hg38UCSC Ensembl
chr20:54940963..54941059hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519929
Supporting Variants
Samples
Known GenesFAM210B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733223
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.129566


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