A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471409



Internal ID21128962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95309677..95317475hg38UCSC Ensembl
chr11:95042841..95050639hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg387799
hg197799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471409
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