A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748089



Internal ID20524113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9640337..9643469hg38UCSC Ensembl
chr8:9497847..9500979hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383133
hg193133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295938
Samples
Known GenesTNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748089
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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