A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194677



Internal ID20761717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16449454..16457235hg38UCSC Ensembl
chr10:16491453..16499234hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387782
hg197782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446492
Supporting Variants
Samples
Known GenesPTER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00053


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