A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942660



Internal ID29108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187381947..187382031hg38UCSC Ensembl
chr3:187099735..187099819hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438005
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942660
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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