A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723390



Internal ID147056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40287312..40290216hg38UCSC Ensembl
chr19:40793219..40796123hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382905
hg192905
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723390
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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