A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017761



Internal ID21927104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48022393..48023467hg38UCSC Ensembl
chr8:48934953..48936027hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597251
Samples
Known GenesUBE2V2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017761
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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