A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763636



Internal ID20539496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89266454..89266454hg38UCSC Ensembl
chr8:90278683..90278683hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763636
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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