A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481155



Internal ID22539059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67199641..67201140hg38UCSC Ensembl
chr1:67665324..67666823hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830622
Supporting Variants
Samples
Known GenesIL23R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481155
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