A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701183



Internal ID124849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47012294..47012448hg38UCSC Ensembl
chr15:47304492..47304646hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701183
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002185


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