A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582968



Internal ID21531486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13514617..13514700hg38UCSC Ensembl
chr3:13556117..13556200hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121081
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582968
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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