A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452311



Internal ID230468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16422123..16427795hg38UCSC Ensembl
chr4:16423746..16429418hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg385673
hg195673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452311
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