A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664097



Internal ID21612402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73950614..73950614hg38UCSC Ensembl
chr13:74524751..74524751hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098869
SamplesNA18534
Known GenesKLF12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664097
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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