A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447233



Internal ID21104786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13020776..13029483hg38UCSC Ensembl
chr11:13042323..13051030hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg388708
hg198708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447233
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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