A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394137



Internal ID21051690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26760757..27463793hg38UCSC Ensembl
chr5:26760866..27463900hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38703037
hg19703035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215746
Samples
Known GenesCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394137
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