A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443048



Internal ID21100601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111691201..111692400hg38UCSC Ensembl
chr9:114453481..114454680hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174605
Samples
Known GenesC9orf84
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer