A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203316



Internal ID20770356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35517700..35525500hg38UCSC Ensembl
chr20:34105529..34113328hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387801
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516004
Supporting Variants
Samples
Known GenesC20orf173
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203316
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