A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120742



Internal ID21453863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98406643..98412478hg38UCSC Ensembl
chr3:98125487..98131322hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg385836
hg195836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581995
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120742
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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