A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457293



Internal ID21114846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89709501..89713100hg38UCSC Ensembl
chr12:90103278..90106877hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194658
Samples
Known GenesLINC00936
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457293
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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