A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971377



Internal ID48260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93261795..93261850hg38UCSC Ensembl
chr5:92597501..92597556hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971377
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