A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458287



Internal ID236316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39760723..39773741hg38UCSC Ensembl
chr4:39762343..39775361hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3813019
hg1913019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948895
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458287
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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