A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067857



Internal ID21977090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89339545..89339545hg38UCSC Ensembl
chr6:90049264..90049264hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569333
Samples
Known GenesUBE2J1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067857
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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