A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582469



Internal ID21530982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123981979..123990770hg38UCSC Ensembl
chr3:123700826..123709617hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg388792
hg198792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121282
SamplesHG03732
Known GenesROPN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582469
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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