A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618316



Internal ID21566621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151678620..151678620hg38UCSC Ensembl
chr4:152599772..152599772hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130270
SamplesNA24385
Known GenesPET112
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618316
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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