A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582780



Internal ID21531296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114241708..114241793hg38UCSC Ensembl
chr5:113577405..113577490hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120489
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582780
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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