A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873883



Internal ID22648832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:124127940..124574242hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38446303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv75n209
Supporting Variantsnssv17364034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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