A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013786



Internal ID21923129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90056945..90057267hg38UCSC Ensembl
chr8:91069173..91069495hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013786
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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