A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142432



Internal ID21487391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115698135..115698135hg38UCSC Ensembl
chr8:116710361..116710361hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632757
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142432
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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