A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124686



Internal ID21506113
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 StatusS
Merged Variantsnsv5608409
Supporting Variants
SamplesNA19983
Known GenesBOD1L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124686
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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