A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684307



Internal ID107973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108436080..108439872hg38UCSC Ensembl
chr12:108829857..108833649hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg383793
hg193793
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684307
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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