A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533826



Internal ID20907187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2873583..2876495hg38UCSC Ensembl
chr18:2873581..2876493hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg382913
hg192913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189447
Samples
Known GenesEMILIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer