A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732880



Internal ID20508806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23590307..23590359hg38UCSC Ensembl
chr8:23447820..23447872hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732880
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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