A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475472



Internal ID21133025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96987089..97009217hg38UCSC Ensembl
chr11:96858089..96880217hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3822129
hg1922129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475472
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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