A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962855



Internal ID42559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16491406..16491655hg38UCSC Ensembl
chr5:16491515..16491764hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454343
Supporting Variants
Samples
Known GenesFAM134B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962855
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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