A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733137



Internal ID20509064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28327795..28328355hg38UCSC Ensembl
chr8:28185312..28185872hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293692
Samples
Known GenesPNOC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733137
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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