A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943049



Internal ID29358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184744009..184744955hg38UCSC Ensembl
chr3:184461797..184462743hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434425
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943049
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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