A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186271



Internal ID20753312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103944079..104113005hg38UCSC Ensembl
chr14:104410416..104579342hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38168927
hg19168927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501420
Supporting Variants
Samples
Known GenesASPG, TDRD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186271
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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