A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865015



Internal ID22639950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:128286123..128288166hg38UCSC Ensembl
chr12:128770668..128772711hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg382044
hg192044
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452958
Samples
Known GenesTMEM132C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865015
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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