A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870472



Internal ID22645408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1492134..1493783hg38UCSC Ensembl
chr20:1472780..1474429hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870472
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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