A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955559



Internal ID22730760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40982057..40983336hg38UCSC Ensembl
chr20:39610697..39611976hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381280
hg191280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955559
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