A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847991



Internal ID22031634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40714012..40714012hg38UCSC Ensembl
chr15:41006210..41006210hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241969
Supporting Variants
Samples
Known GenesRAD51
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847991
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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