A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602377



Internal ID21551035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113737293..113737384hg38UCSC Ensembl
chr13:114440266..114440357hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092898
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602377
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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