A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720895



Internal ID144561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6093359..6096890hg38UCSC Ensembl
chr19:6093370..6096901hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383532
hg193532
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557412
Supporting Variants
Samples
Known GenesRFX2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720895
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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