A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017379



Internal ID21926722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85178453..85179005hg38UCSC Ensembl
chr8:86090688..86091240hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578038
Samples
Known GenesE2F5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017379
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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