A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092219



Internal ID21431970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38925484..38925484hg38UCSC Ensembl
chr13:39499621..39499621hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647978
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092219
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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