A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427088



Internal ID21084641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28467668..28796272hg38UCSC Ensembl
chr9:28467666..28796270hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38328605
hg19328605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183330
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427088
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