A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018828



Internal ID21928171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90631705..90645111hg38UCSC Ensembl
chr8:91643933..91657339hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3813407
hg1913407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590385
Samples
Known GenesTMEM64
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018828
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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