A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720341



Internal ID144007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2090806..2093261hg38UCSC Ensembl
chr19:2090805..2093260hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382456
hg192456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519673
Supporting Variants
Samples
Known GenesMOB3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720341
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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