A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859113



Internal ID22634048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94515629..94516828hg38UCSC Ensembl
chr14:94981966..94983165hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470146, nssv17470377
Samples
Known GenesSERPINA12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859113
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