A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733026



Internal ID156692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53129783..53129904hg38UCSC Ensembl
chr20:51746322..51746443hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520213
Supporting Variants
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733026
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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