A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459791



Internal ID21117344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120021352..120124725hg38UCSC Ensembl
chr11:119892061..119995433hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38103374
hg19103373
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181785
Samples
Known GenesTRIM29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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