A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383193



Internal ID21040746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62799301..62832400hg38UCSC Ensembl
chr4:63665019..63698118hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3833100
hg1933100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5281n223
Supporting Variantsnssv18210934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383193
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