A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437160



Internal ID21094713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89561101..89564100hg38UCSC Ensembl
chr9:92176016..92179015hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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