A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846898



Internal ID22030541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69518683..69518683hg38UCSC Ensembl
chr15:69811022..69811022hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846898
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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