A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459568



Internal ID237581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177441174..177441980hg38UCSC Ensembl
chr4:178362328..178363134hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959389
Samples
Known GenesAGA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459568
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