A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470308



Internal ID21127861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68622101..68717400hg38UCSC Ensembl
chr11:68389569..68484868hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3895300
hg1995300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1222n223
Supporting Variantsnssv18178870
Samples
Known GenesGAL, MTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470308
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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