A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086309



Internal ID21478534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80152695..80152760hg38UCSC Ensembl
chr15:80445037..80445102hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602245
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086309
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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