A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019382



Internal ID21928725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76365912..76366765hg38UCSC Ensembl
chr8:77278147..77279000hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595420
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019382
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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