A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618128



Internal ID21566433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153247983..153247983hg38UCSC Ensembl
chr4:154169135..154169135hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125795
SamplesHG00513
Known GenesTRIM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618128
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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