A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721268



Internal ID144934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9938050..9938993hg38UCSC Ensembl
chr19:10048726..10049669hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721268
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00643


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