A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403094



Internal ID22460964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7288958..7289601hg38UCSC Ensembl
chr20:7269605..7270248hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403094
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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