A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454417



Internal ID21111970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120630801..120640700hg38UCSC Ensembl
chr9:123393079..123402978hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232569
Samples
Known GenesMEGF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454417
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