A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611254



Internal ID21559559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137555888..137555888hg38UCSC Ensembl
chr4:138477042..138477042hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127792
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611254
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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