A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846818



Internal ID22030461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32662495..32662495hg38UCSC Ensembl
chr15:32954696..32954696hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241874
Supporting Variants
Samples
Known GenesSCG5
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846818
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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