A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092639



Internal ID21501336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111670758..111670758hg38UCSC Ensembl
chr13:112323105..112323105hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660817
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092639
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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