A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080609



Internal ID21490189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38856738..38856738hg38UCSC Ensembl
chr13:39430875..39430875hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659835
Supporting Variants
SamplesNA19238
Known GenesFREM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080609
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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