A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846682



Internal ID22030325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58064921..58064921hg38UCSC Ensembl
chr15:58357119..58357119hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249708
Supporting Variants
Samples
Known GenesALDH1A2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846682
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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