A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038443



Internal ID21947786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110515508..110518035hg38UCSC Ensembl
chr12:110953313..110955840hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382528
hg192528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613932
Samples
Known GenesRAD9B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038443
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