A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009985



Internal ID21919328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6373068..6373235hg38UCSC Ensembl
chr8:6230589..6230756hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009985
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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