A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447441



Internal ID21104994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41922501..41953500hg38UCSC Ensembl
chr9:65602489..65633478hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3831000
hg1930990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230510
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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