A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535203



Internal ID20908564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45652348..45724710hg38UCSC Ensembl
chr19:46155606..46227968hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3872363
hg1972363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198894
Samples
Known GenesFBXO46, GIPR, MIR642A, MIR642B, QPCTL, SNRPD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535203
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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