A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529164



Internal ID20902525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68847018..68940106hg38UCSC Ensembl
chr18:66514255..66607343hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3893089
hg1993089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197616
Samples
Known GenesCCDC102B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529164
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