A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149918



Internal ID21468580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116579230..116579524hg38UCSC Ensembl
chr8:117591469..117591763hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567051
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149918
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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