A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467300



Internal ID21124853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63569202..63571681hg38UCSC Ensembl
chr11:63336674..63339153hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382480
hg192480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467300
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