A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093606



Internal ID21478319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86311548..86311548hg38UCSC Ensembl
chr13:86963803..86963803hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653875
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093606
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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