A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531753



Internal ID20905114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36697411..37375336hg38UCSC Ensembl
chr18:34277374..34955299hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38677926
hg19677926
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185625
Samples
Known GenesCELF4, FHOD3, KIAA1328, TPGS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531753
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