A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445564



Internal ID21103117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97012501..97015600hg38UCSC Ensembl
chr9:99774783..99777882hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223332
Samples
Known GenesHIATL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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