A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451119



Internal ID21108672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113846811..113858789hg38UCSC Ensembl
chr9:116609091..116621069hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3811979
hg1911979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7919n223
Supporting Variantsnssv18223675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451119
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