A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498863



Internal ID275845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24997172..25001085hg38UCSC Ensembl
chr15:25242319..25246232hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383914
hg193914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498863
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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