A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471362



Internal ID21128915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93279501..93295800hg38UCSC Ensembl
chr11:93012667..93028966hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3816300
hg1916300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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