A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565091



Internal ID21513401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190965996..190966138hg38UCSC Ensembl
chr3:190683785..190683927hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129934
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565091
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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