A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123812



Internal ID21488087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32169748..32169827hg38UCSC Ensembl
chr3:32211240..32211319hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571381
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123812
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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