A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463924



Internal ID21121477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129893001..129898300hg38UCSC Ensembl
chr11:129762896..129768195hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186402
Samples
Known GenesNFRKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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