A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884465



Internal ID22659448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183828351..183834184hg38UCSC Ensembl
chr1:183797485..183803318hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385834
hg195834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360710
Samples
Known GenesRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884465
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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