A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459402



Internal ID21116955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65202237..65204307hg38UCSC Ensembl
chr11:64969708..64971778hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382071
hg192071
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194290
Samples
Known GenesCAPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459402
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