A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459973



Internal ID22517859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102384799..102387123hg38UCSC Ensembl
chr14:102851136..102853460hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382325
hg192325
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860519
Supporting Variants
Samples
Known GenesTECPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459973
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