A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451474



Internal ID21109027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133062101..133067300hg38UCSC Ensembl
chr9:135937488..135942687hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7955n223
Supporting Variantsnssv18235851
Samples
Known GenesCEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451474
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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