A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906513



Internal ID22681714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102840897..102842989hg38UCSC Ensembl
chr4:103762054..103764146hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428088
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906513
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer