A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459837



Internal ID21117390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43174724..43182558hg38UCSC Ensembl
chr11:43196274..43204108hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387835
hg197835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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