A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933534



Internal ID23094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54639695..54643527hg38UCSC Ensembl
chr3:54673722..54677554hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg383833
hg193833
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563420
Supporting Variants
Samples
Known GenesCACNA2D3, ESRG
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933534
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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