A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846897



Internal ID22030540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69508528..69508528hg38UCSC Ensembl
chr15:69800867..69800867hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846897
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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