A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127760



Internal ID21489238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86248389..86248564hg38UCSC Ensembl
chr3:86297539..86297714hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565237
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127760
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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