A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459646



Internal ID21117199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63344567..63439660hg38UCSC Ensembl
chr11:63112039..63207132hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3895094
hg1995094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179403
Samples
Known GenesMIR3680-1, MIR3680-2, SLC22A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459646
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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