A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439962



Internal ID21097515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30321025..30334443hg38UCSC Ensembl
chr11:30342572..30355990hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3813419
hg1913419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179226
Samples
Known GenesARL14EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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