A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472441



Internal ID21129994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33703723..33707820hg38UCSC Ensembl
chr11:33725269..33729366hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384098
hg194098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189811
Samples
Known GenesCD59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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