A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732229



Internal ID20508153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43743453..43743606hg38UCSC Ensembl
chr21:45163334..45163487hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295728
Samples
Known GenesPDXK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732229
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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