A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522370



Internal ID20895731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18921011..18936249hg38UCSC Ensembl
chr19:19031820..19047058hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3815239
hg1915239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198359
Samples
Known GenesDDX49, HOMER3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522370
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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