A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621839



Internal ID21570144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14389725..14389725hg38UCSC Ensembl
chr4:14391349..14391349hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134221
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621839
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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