A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264832



Internal ID20474050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81517190..81517281hg38UCSC Ensembl
chr16:81550795..81550886hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744981
Supporting Variants
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264832
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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