A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451071



Internal ID21108624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24769696..24888423hg38UCSC Ensembl
chr11:24791242..24909969hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38118728
hg19118728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187285
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451071
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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