A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877390



Internal ID22652354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165452569..165454961hg38UCSC Ensembl
chr1:165421806..165424198hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382393
hg192393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877390
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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