A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731530



Internal ID155196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21346863..21347073hg38UCSC Ensembl
chr20:21327501..21327711hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521038
Supporting Variants
Samples
Known GenesXRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731530
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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