A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390199



Internal ID21047752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139604745..139700680hg38UCSC Ensembl
chr4:140525899..140621834hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3895936
hg1995936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213043
Samples
Known GenesMGST2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390199
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