A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024085



Internal ID21933428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67843856..67845010hg38UCSC Ensembl
chr12:68237636..68238790hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024085
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