A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128318



Internal ID21478771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174289957..174289957hg38UCSC Ensembl
chr3:174007747..174007747hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621253
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128318
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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