A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942095



Internal ID28744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164810610..164837887hg38UCSC Ensembl
chr3:164528398..164555675hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3827278
hg1927278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942095
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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