A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461622



Internal ID21119175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122406773..122410791hg38UCSC Ensembl
chr11:122277481..122281499hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg384019
hg194019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer