A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385773



Internal ID22443643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29983382..29983382hg38UCSC Ensembl
chr14:30452588..30452588hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385773
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer