A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467449



Internal ID21125002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112202301..112208400hg38UCSC Ensembl
chr11:112073024..112079123hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186978
Samples
Known GenesBCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467449
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