A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457687



Internal ID235726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56013222..56017584hg38UCSC Ensembl
chr5:55309050..55313412hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg384363
hg194363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457687
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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