A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958550



Internal ID22733612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37125228..37125870hg38UCSC Ensembl
chr20:35753631..35754273hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399336
Samples
Known GenesMROH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958550
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