A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464259



Internal ID21121812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50709501..50821300hg38UCSC Ensembl
chr11:50668672..50780471hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38111800
hg19111800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1143n223
Supporting Variantsnssv18181210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464259
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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