A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731868



Internal ID20507789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66521799..66521854hg38UCSC Ensembl
chr8:67434034..67434089hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731868
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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