A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721260



Internal ID144926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9819398..9820570hg38UCSC Ensembl
chr19:9930074..9931246hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721260
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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