A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703176



Internal ID126842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60634139..60634190hg38UCSC Ensembl
chr15:60926338..60926389hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg386007
hg196007
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562240
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703176
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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