A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767223



Internal ID20543083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34229165..34229165hg38UCSC Ensembl
chr21:35601466..35601466hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767223
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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