A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17470379



Internal ID22528269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94629977..94638955hg38UCSC Ensembl
chr14:95096314..95105292hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg388979
hg198979
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861946
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17470379
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