A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503424



Internal ID280251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131112883..131355680hg38UCSC Ensembl
chr12:131597428..131840225hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38242798
hg19242798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17685500
Samples
Known GenesGPR133, LOC116437, LOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503424
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