A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462701



Internal ID240625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39702771..39712236hg38UCSC Ensembl
chr4:39704391..39713856hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg389466
hg199466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948884
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462701
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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