A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533794



Internal ID20907155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46666686..46685385hg38UCSC Ensembl
chr19:47169943..47188642hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3818700
hg1918700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198918
Samples
Known GenesDACT3-AS1, PRKD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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