A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016565



Internal ID21925908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53305056..53305159hg38UCSC Ensembl
chr6:53169854..53169957hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567314
Samples
Known GenesELOVL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016565
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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