A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445069



Internal ID21102622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81607544..81608359hg38UCSC Ensembl
chr9:84222459..84223274hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190308
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445069
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