A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281632



Internal ID20490850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23665973..23666051hg38UCSC Ensembl
chr16:23677294..23677372hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739672
Supporting Variants
Samples
Known GenesDCTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281632
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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