A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721843



Internal ID145509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16194859..16205758hg38UCSC Ensembl
chr19:16305670..16316569hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530040
Supporting Variants
Samples
Known GenesAP1M1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721843
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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