A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457975



Internal ID21115528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79674088..79674473hg38UCSC Ensembl
chr11:79385132..79385517hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457975
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