A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026833



Internal ID21936176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:128170950..128171023hg38UCSC Ensembl
chr12:128655495..128655568hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026833
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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