A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020421



Internal ID21929764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10734036..10734099hg38UCSC Ensembl
chr8:10591546..10591609hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020421
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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