A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459734



Internal ID237744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39539359..39544046hg38UCSC Ensembl
chr4:39540979..39545666hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384688
hg194688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947260
Samples
Known GenesMIR1273H, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459734
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