A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090907



Internal ID21491803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26281566..26281566hg38UCSC Ensembl
chr13:26855703..26855703hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656050
Supporting Variants
SamplesNA19238
Known GenesCDK8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090907
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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