A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702833



Internal ID126499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62453047..62456934hg38UCSC Ensembl
chr15:62745246..62749133hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383888
hg193888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702833
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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