A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463149



Internal ID21120702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58777503..58909891hg38UCSC Ensembl
chr11:58544976..58677364hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38132389
hg19132389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178030
Samples
Known GenesGLYATL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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