A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749432



Internal ID20525463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129041530..129041596hg38UCSC Ensembl
chr8:130053776..130053842hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749432
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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