A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720873



Internal ID144539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5831859..5859706hg38UCSC Ensembl
chr19:5831870..5859717hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3827848
hg1927848
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560506
Supporting Variants
Samples
Known GenesFUT3, FUT6
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720873
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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