A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962173



Internal ID42079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17288998..17298823hg38UCSC Ensembl
chr5:17289107..17298932hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg389826
hg199826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465694
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962173
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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