A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086508



Internal ID21487068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113215050..113215050hg38UCSC Ensembl
chr13:113869364..113869364hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661534
Supporting Variants
SamplesNA12878
Known GenesCUL4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086508
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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