A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846856



Internal ID22030499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63526592..63526592hg38UCSC Ensembl
chr15:63818791..63818791hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249753
Supporting Variants
Samples
Known GenesUSP3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846856
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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