A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084042



Internal ID21509872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109489241..109489241hg38UCSC Ensembl
chr13:110141588..110141588hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662039
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084042
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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