A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450296



Internal ID21107849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23003556..24846291hg38UCSC Ensembl
chr11:23025102..24867837hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg381842736
hg191842736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183494
Samples
Known GenesLUZP2, MIR8054
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450296
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