A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661883



Internal ID21610188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38822393..38822393hg38UCSC Ensembl
chr13:39396530..39396530hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092218
SamplesHG02587
Known GenesFREM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661883
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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