A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934318



Internal ID23609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78327401..78585274hg38UCSC Ensembl
chr3:78376551..78634424hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38257874
hg19257874
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559528
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934318
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.022791


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