A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533382



Internal ID20906743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4134766..4135405hg38UCSC Ensembl
chr18:4134766..4135405hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183100
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533382
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