A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464746



Internal ID21122299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119333685..119352569hg38UCSC Ensembl
chr11:119204395..119223279hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3818885
hg1918885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187905
Samples
Known GenesC1QTNF5, MFRP, RNF26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464746
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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