A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466169



Internal ID244015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178195320..178195624hg38UCSC Ensembl
chr5:177622321..177622625hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466169
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