A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583931



Internal ID21532462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44510749..44510798hg38UCSC Ensembl
chr3:44552241..44552290hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133823
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583931
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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