A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458677



Internal ID21116230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117107296..117121705hg38UCSC Ensembl
chr11:116978012..116992421hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3814410
hg1914410
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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