A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408588



Internal ID21066141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180267372..180298522hg38UCSC Ensembl
chr5:179694372..179725522hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3831151
hg1931151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215131
Samples
Known GenesMAPK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408588
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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