A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472555



Internal ID21130108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89299159..89322350hg38UCSC Ensembl
chr11:89032327..89055518hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3823192
hg1923192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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