A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619133



Internal ID21567438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76460827..76460827hg38UCSC Ensembl
chr4:77381980..77381980hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135771
SamplesNA12878
Known GenesSHROOM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619133
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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