A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460811



Internal ID21118364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121637582..121643387hg38UCSC Ensembl
chr11:121508291..121514096hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg385806
hg195806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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