A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445221



Internal ID21102774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17533224..17716533hg38UCSC Ensembl
chr11:17554771..17738080hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38183310
hg19183310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181242
Samples
Known GenesOTOG, USH1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445221
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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