A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17470365



Internal ID22528255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94316520..94335152hg38UCSC Ensembl
chr14:94782857..94801489hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3818633
hg1918633
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854102
Supporting Variants
Samples
Known GenesSERPINA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17470365
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