A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967983



Internal ID45973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84460887..84491585hg38UCSC Ensembl
chr5:83756705..83787403hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3830699
hg1930699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967983
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004528


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