A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014483



Internal ID21923826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169963840..169963892hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014483
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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