A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618120



Internal ID21566425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39348466..39348466hg38UCSC Ensembl
chr4:39350086..39350086hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130883
SamplesHG00732
Known GenesMIR1273H, RFC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618120
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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