A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932957



Internal ID22694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47482859..47491688hg38UCSC Ensembl
chr3:47524349..47533178hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg388830
hg198830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447607
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932957
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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