A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967184



Internal ID45436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76344436..76348771hg38UCSC Ensembl
chr5:75640261..75644596hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg384336
hg194336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967184
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer