A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900101



Internal ID852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22883659..22883710hg38UCSC Ensembl
chr1:23210152..23210203hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395606
Supporting Variants
Samples
Known GenesEPHB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900101
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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