A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395403



Internal ID21052956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128851444..129013507hg38UCSC Ensembl
chr4:129772599..129934662hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38162064
hg19162064
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210315
Samples
Known GenesJADE1, SCLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395403
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