A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136942



Internal ID21478751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125297423..125297750hg38UCSC Ensembl
chr3:125016267..125016594hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572131
Supporting Variants
SamplesHG03486
Known GenesZNF148
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136942
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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