A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388711



Internal ID21046264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43397559..43408837hg38UCSC Ensembl
chr5:43397661..43408939hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3811279
hg1911279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214113
Samples
Known GenesCCL28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388711
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