A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936067



Internal ID24758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73833624..73833716hg38UCSC Ensembl
chr3:73882775..73882867hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936067
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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