A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459397



Internal ID21116950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66957301..66958900hg38UCSC Ensembl
chr11:66724772..66726371hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189480
Samples
Known GenesPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459397
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