A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704373



Internal ID128039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79064862..79064913hg38UCSC Ensembl
chr15:79357204..79357255hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418075
Supporting Variants
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704373
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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