A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760541



Internal ID20536401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89339585..89339585hg38UCSC Ensembl
chr6:90049304..90049304hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288254
Samples
Known GenesUBE2J1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760541
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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