A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931695



Internal ID21866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44454013..44454050hg38UCSC Ensembl
chr3:44495505..44495542hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398007
Supporting Variants
Samples
Known GenesZNF445
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931695
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002498


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