A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648511



Internal ID21596816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52622289..52622289hg38UCSC Ensembl
chr13:53196424..53196424hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080757
SamplesHG03065
Known GenesHNRNPA1L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648511
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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