A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469665



Internal ID21127218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66672662..66674844hg38UCSC Ensembl
chr11:66440133..66442315hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382183
hg192183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196092
Samples
Known GenesRBM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469665
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