A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962106



Internal ID42036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16845153..16845243hg38UCSC Ensembl
chr5:16845262..16845352hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472186
Supporting Variants
Samples
Known GenesMYO10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962106
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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