A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460634



Internal ID21118187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42586041..42586598hg38UCSC Ensembl
chr11:42607591..42608148hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460634
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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