A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943212



Internal ID29455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172455536..172456236hg38UCSC Ensembl
chr3:172173326..172174026hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943212
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.148142


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