A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460475



Internal ID21118028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116746040..116747122hg38UCSC Ensembl
chr11:116616756..116617838hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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