A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186871



Internal ID20753911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74942126..74953184hg38UCSC Ensembl
chr14:75408829..75419887hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3811059
hg1911059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488589
Supporting Variants
Samples
Known GenesPGF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186871
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