A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525369



Internal ID20898730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42041284..42133594hg38UCSC Ensembl
chr18:39621248..39713558hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3892311
hg1992311
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189539
Samples
Known GenesPIK3C3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525369
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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