A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940192



Internal ID27505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161266486..161273582hg38UCSC Ensembl
chr3:160984274..160991370hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg387097
hg197097
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940192
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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