A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938951



Internal ID26686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145805573..145805573hg38UCSC Ensembl
chr3:145523360..145523360hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938951
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.043568


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