A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652682



Internal ID21600987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108215427..108215427hg38UCSC Ensembl
chr13:108867775..108867775hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096702
SamplesHG00731
Known GenesLIG4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652682
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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