A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391282



Internal ID21048835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103932701..103938100hg38UCSC Ensembl
chr4:104853858..104859257hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391282
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