A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460245



Internal ID238236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155497928..155498525hg38UCSC Ensembl
chr4:156419080..156419677hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460245
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