A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581427



Internal ID21529926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155301378..155302031hg38UCSC Ensembl
chr4:156222530..156223183hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121872
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581427
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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