A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442566



Internal ID21100119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20896571..20917166hg38UCSC Ensembl
chr11:20918117..20938712hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3820596
hg1920596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195978
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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