A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094691



Internal ID21451955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67368598..67368598hg38UCSC Ensembl
chr13:67942730..67942730hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg386491
hg196491
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652098
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094691
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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