A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523009



Internal ID299259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77924606..78018356hg38UCSC Ensembl
chr15:78216948..78310698hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3893751
hg1993751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702160
Samples
Known GenesLOC645752, LOC91450, TBC1D2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523009
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer