A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084082



Internal ID21403277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100719113..100719241hg38UCSC Ensembl
chr15:101259318..101259446hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588087
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084082
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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