A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135814



Internal ID21489292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23850988..23850988hg38UCSC Ensembl
chr3:23892479..23892479hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382139
hg192139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613821
Supporting Variants
SamplesNA18939
Known GenesUBE2E1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135814
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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