A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967964



Internal ID45961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84157741..84164469hg38UCSC Ensembl
chr5:83453559..83460287hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386729
hg196729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460597
Supporting Variants
Samples
Known GenesEDIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967964
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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