A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533523



Internal ID20906884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45438025..45519713hg38UCSC Ensembl
chr19:45941283..46022971hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3881689
hg1981689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198883
Samples
Known GenesFOSB, PPM1N, RTN2, VASP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533523
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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