A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743036



Internal ID20519022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92777534..92780384hg38UCSC Ensembl
chr8:93789762..93792612hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382851
hg192851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291828
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743036
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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