A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459250



Internal ID21116803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130036918..130038907hg38UCSC Ensembl
chr11:129906813..129908802hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459250
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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