A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089286



Internal ID21998519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75234441..75234441hg38UCSC Ensembl
chr12:75628221..75628221hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089286
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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