A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449268



Internal ID21106821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66721201..66722500hg38UCSC Ensembl
chr9:41799481..41800779hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg381300
hg191299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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