A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870573



Internal ID22645509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53388649..53393066hg38UCSC Ensembl
chr1:53854321..53858738hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384418
hg194418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870573
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