A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460286



Internal ID21117839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128437201..128448600hg38UCSC Ensembl
chr11:128307096..128318495hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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