A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158578



Internal ID21478691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80232466..80232703hg38UCSC Ensembl
chr8:81144701..81144938hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565589
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158578
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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