A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976314



Internal ID51605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147869844..147874156hg38UCSC Ensembl
chr5:147249407..147253719hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg384313
hg194313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976314
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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