A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931320



Internal ID21632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25485517..25487476hg38UCSC Ensembl
chr3:25527008..25528967hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444893
Supporting Variants
Samples
Known GenesRARB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931320
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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