A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909067



Internal ID22684277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78771162..78771250hg38UCSC Ensembl
chr8:79683397..79683485hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432810
Samples
Known GenesIL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909067
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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