A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608409



Internal ID21556714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13596049..13596049hg38UCSC Ensembl
chr4:13597673..13597673hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124686
SamplesNA19983
Known GenesBOD1L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608409
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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