A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451722



Internal ID21109275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8592001..8599500hg38UCSC Ensembl
chr11:8613548..8621047hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188023
Samples
Known GenesSTK33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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