A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997194



Internal ID21906537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39705788..39705941hg38UCSC Ensembl
chr4:39707408..39707561hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539556
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997194
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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