A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943692



Internal ID29775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180165492..180165641hg38UCSC Ensembl
chr3:179883280..179883429hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437948
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943692
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.021542


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