A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459354



Internal ID21116907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60613901..60626800hg38UCSC Ensembl
chr11:60381374..60394273hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3812900
hg1912900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1202n223
Supporting Variantsnssv18181810
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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