A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723006



Internal ID146672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35350593..35362945hg38UCSC Ensembl
chr19:35841496..35853847hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812353
hg1912352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144711
Supporting Variants
Samples
Known GenesFFAR1, FFAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723006
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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