A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866817



Internal ID22641752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72871330..72875529hg38UCSC Ensembl
chr8:73783565..73787764hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509842
Samples
Known GenesKCNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866817
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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