A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569333



Internal ID21761376
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 StatusS
Merged Variantsnsv6067857
Supporting Variants
Samples
Known GenesUBE2J1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569333
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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