A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937543



Internal ID25748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108000975..108023284hg38UCSC Ensembl
chr3:107719822..107742131hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3822310
hg1922310
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937543
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.003903


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