A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522984



Internal ID20896345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32882889..32888840hg38UCSC Ensembl
chr19:33373795..33379746hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg385952
hg195952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197314
Samples
Known GenesCEP89
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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