A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032166



Internal ID21941509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86225359..86231821hg38UCSC Ensembl
chr16:86258965..86265427hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386463
hg196463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624428
Samples
Known GenesLINC01081
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032166
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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