A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966689



Internal ID45111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67645807..67647894hg38UCSC Ensembl
chr5:66941635..66943722hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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