A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936084



Internal ID24770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74182698..74184221hg38UCSC Ensembl
chr3:74231849..74233372hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936084
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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