A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944672



Internal ID30461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180828382..180828499hg38UCSC Ensembl
chr3:180546170..180546287hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446131
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944672
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002654


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