A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603892



Internal ID21552559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75894812..75894874hg38UCSC Ensembl
chr13:76468948..76469010hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096671
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603892
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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