A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721654



Internal ID145320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14098000..14136000hg38UCSC Ensembl
chr19:14208812..14246812hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3838001
hg1938001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144910
Supporting Variants
Samples
Known GenesASF1B, PRKACA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721654
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002093


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