A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846660



Internal ID22030303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55682036..55682036hg38UCSC Ensembl
chr15:55974234..55974234hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242118
Supporting Variants
Samples
Known GenesPRTG
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846660
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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