A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627239



Internal ID21819286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86278798..86278988hg38UCSC Ensembl
chr16:86312404..86312594hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028899
Supporting Variants
Samples
Known GenesLINC01081
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627239
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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