A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447928



Internal ID21105481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128015024..128033051hg38UCSC Ensembl
chr9:130777303..130795330hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3818028
hg1918028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447928
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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