A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452047



Internal ID21109600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33864831..33874936hg38UCSC Ensembl
chr9:33864829..33874934hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3810106
hg1910106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234546
Samples
Known GenesUBE2R2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452047
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