A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528215



Internal ID20901576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68745401..68877100hg38UCSC Ensembl
chr18:66412638..66544337hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38131700
hg19131700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197615
Samples
Known GenesCCDC102B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528215
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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