A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430339



Internal ID209151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26252909..26252960hg38UCSC Ensembl
chr12:26405842..26405893hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17055438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430339
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