A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460867



Internal ID22518750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102573148..102581040hg38UCSC Ensembl
chr14:103039485..103047377hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg387893
hg197893
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460867
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