A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448286



Internal ID21105839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86967659..86970257hg38UCSC Ensembl
chr9:89582574..89585172hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180722
Samples
Known GenesLOC100506834
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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