A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639119



Internal ID21587424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184826087..184826087hg38UCSC Ensembl
chr4:185747241..185747241hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134740
SamplesHG02492
Known GenesACSL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639119
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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