A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410604



Internal ID21068157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96650762..96744663hg38UCSC Ensembl
chr5:95986466..96080367hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3893902
hg1993902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215437
Samples
Known GenesCAST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410604
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