A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634921



Internal ID21826968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69374627..69374685hg38UCSC Ensembl
chr16:69408530..69408588hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029116
Supporting Variants
Samples
Known GenesTERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634921
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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