A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982105



Internal ID21891448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183659713..183668286hg38UCSC Ensembl
chr1:183628848..183637421hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg388574
hg198574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530162
Samples
Known GenesRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982105
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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