A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704973



Internal ID128639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10632876..10636103hg38UCSC Ensembl
chr16:10726733..10729960hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383228
hg193228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516788
Supporting Variants
Samples
Known GenesTEKT5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704973
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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