A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462314



Internal ID21119867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123137228..123142757hg38UCSC Ensembl
chr11:123007936..123013465hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg385530
hg195530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179931
Samples
Known GenesCLMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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