A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457092



Internal ID235147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88422596..88426997hg38UCSC Ensembl
chr4:89343748..89348149hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg384402
hg194402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951583
Samples
Known GenesHERC6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457092
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