A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107125



Internal ID22016358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32283763..32283763hg38UCSC Ensembl
chr21:33656074..33656074hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107125
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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