A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720913



Internal ID144579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6296866..6331498hg38UCSC Ensembl
chr19:6296877..6331509hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3834633
hg1934633
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559908
Supporting Variants
Samples
Known GenesACER1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720913
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.051983


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer