A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543459



Internal ID20916707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41877601..41879900hg38UCSC Ensembl
chr21:43297710..43300009hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203982
Samples
Known GenesPRDM15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543459
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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