A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436599



Internal ID215212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25218470..25232206hg38UCSC Ensembl
chr4:25220092..25233828hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3813737
hg1913737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436599
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