A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017493



Internal ID21926836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101187852..101187931hg38UCSC Ensembl
chr8:102200080..102200159hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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