A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444225



Internal ID21101778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65543201..65563600hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3820400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7800n223
Supporting Variantsnssv18234716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444225
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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