A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120898



Internal ID21466906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32652838..32653877hg38UCSC Ensembl
chr3:32694330..32695369hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381040
hg191040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584060
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120898
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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