A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016515



Internal ID21925858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10938252..10938361hg38UCSC Ensembl
chr8:10795762..10795871hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572846
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016515
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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