A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848661



Internal ID22032304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74589049..74589049hg38UCSC Ensembl
chr15:74881390..74881390hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249831
Supporting Variants
Samples
Known GenesARID3B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848661
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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