A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450997



Internal ID21108550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3174583..3207034hg38UCSC Ensembl
chr11:3195813..3228264hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3832452
hg1932452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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