A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582893



Internal ID21531410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20320746..20320818hg38UCSC Ensembl
chr6:20320977..20321049hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143809
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582893
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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