A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583894



Internal ID21532425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11166706..11166807hg38UCSC Ensembl
chr3:11208392..11208493hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120077
SamplesNA24385
Known GenesHRH1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583894
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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