A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455568



Internal ID233647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80249079..80249602hg38UCSC Ensembl
chr5:79544898..79545421hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967301
Samples
Known GenesSERINC5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455568
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