A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194051



Internal ID20761091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47642501..47732000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3889500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194051
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0555


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