A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855711



Internal ID22039354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69017916..69017916hg38UCSC Ensembl
chr3:69067067..69067067hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855711
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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