A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664841



Internal ID21613148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112998712..113007517hg38UCSC Ensembl
chr13:113653026..113661831hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg388806
hg198806
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089780
SamplesNA19239
Known GenesMCF2L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664841
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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