A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523791



Internal ID20897152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14371301..14499100hg38UCSC Ensembl
chr18:14371300..14499099hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38127800
hg19127800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3316n223
Supporting Variantsnssv18178479
Samples
Known GenesCXADRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523791
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