A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408038



Internal ID22465908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4290198..4293738hg38UCSC Ensembl
chr20:4270845..4274385hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383541
hg193541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934402
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408038
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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