A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739366



Internal ID20515339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45268811..45268865hg38UCSC Ensembl
chr21:46688726..46688780hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265646
Samples
Known GenesPOFUT2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739366
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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