A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032287



Internal ID21941630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66032016..66032530hg38UCSC Ensembl
chr12:66425796..66426310hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032287
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