A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463233



Internal ID241141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86182147..86208963hg38UCSC Ensembl
chr4:87103300..87130116hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3826817
hg1926817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953194
Samples
Known GenesMAPK10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463233
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