A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488314



Internal ID22546231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165629844..165632115hg38UCSC Ensembl
chr2:166486354..166488625hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382272
hg192272
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831417
Supporting Variants
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488314
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