A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188825



Internal ID20755865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45888701..46309200hg38UCSC Ensembl
chr14:46357904..46778403hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38420500
hg19420500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483788
Supporting Variants
Samples
Known GenesLINC00871
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188825
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00026


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