A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584478



Internal ID21533019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43338022..43338110hg38UCSC Ensembl
chr4:43340039..43340127hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135704
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584478
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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