A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456991



Internal ID21114544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69911904..69925788hg38UCSC Ensembl
chr11_gl000202_random:9157..23225hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3813885
hg1914069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456991
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