A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016570



Internal ID21925913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73743768..73745468hg38UCSC Ensembl
chr8:74656003..74657703hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584940
Samples
Known GenesSTAU2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016570
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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