A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846826



Internal ID22030469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60637097..60637097hg38UCSC Ensembl
chr15:60929296..60929296hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249723
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846826
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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