A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446489



Internal ID21104042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86682638..86685892hg38UCSC Ensembl
chr9:89297553..89300807hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg383255
hg193255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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