A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462413



Internal ID21119966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123129945..123152626hg38UCSC Ensembl
chr11:123000653..123023334hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3822682
hg1922682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182314
Samples
Known GenesCLMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462413
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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