A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320963



Internal ID20854064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19111688..19192016hg38UCSC Ensembl
chr1:19438182..19518510hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3880329
hg1980329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199809
Samples
Known GenesUBR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320963
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