A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531624



Internal ID307579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72859900..72869828hg38UCSC Ensembl
chr15:73152241..73162169hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg389929
hg199929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531624
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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