A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452406



Internal ID21109959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89462429..90301103hg38UCSC Ensembl
chr9:92077344..93063385hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38838675
hg19986042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223008
Samples
Known GenesGADD45G, LOC286370, MIR4290, SEMA4D, UNQ6494
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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