A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281418



Internal ID20490636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58710710..58710795hg38UCSC Ensembl
chr16:58744614..58744699hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733914
Supporting Variants
Samples
Known GenesGOT2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281418
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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