A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469855



Internal ID21127408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65518042..65544547hg38UCSC Ensembl
chr11:65285513..65312018hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3826506
hg1926506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183717
Samples
Known GenesLTBP3, SCYL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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