A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522997



Internal ID20896358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68680803..68756893hg38UCSC Ensembl
chr18:66348040..66424130hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3876091
hg1976091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197611
Samples
Known GenesCCDC102B, TMX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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