A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530116



Internal ID20903477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4136112..4159310hg38UCSC Ensembl
chr19:4136109..4159307hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3823199
hg1923199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198811
Samples
Known GenesCREB3L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530116
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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