A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470689



Internal ID21128242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33981121..33991970hg38UCSC Ensembl
chr11:34002668..34013517hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3810850
hg1910850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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