A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578223



Internal ID21526687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166191672..166191733hg38UCSC Ensembl
chr2:167048182..167048243hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110394
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578223
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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