A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517404



Internal ID293828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78732874..78747200hg38UCSC Ensembl
chr15:79025216..79039542hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3814327
hg1914327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517404
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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