A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580260



Internal ID21528748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122789281..122789336hg38UCSC Ensembl
chr4:123710436..123710491hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132562
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580260
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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