A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853304



Internal ID22036947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25503446..25503446hg38UCSC Ensembl
chr3:25544937..25544937hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253839
Supporting Variants
Samples
Known GenesRARB
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853304
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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