A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933976



Internal ID23383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66147250..66245705hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3898456
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933976
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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