A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135641



Internal ID21468979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8655159..8655159hg38UCSC Ensembl
chr3:8696845..8696845hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624498
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135641
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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