A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418515



Internal ID21076068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13483218..13507263hg38UCSC Ensembl
chr9:13483217..13507262hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3824046
hg1924046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418515
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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