A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202186



Internal ID20769226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14122640..14211237hg38UCSC Ensembl
chr20:14103286..14191883hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3888598
hg1988598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527357
Supporting Variants
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202186
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