A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107827



Internal ID22017061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46382956..46382956hg38UCSC Ensembl
chr21:47802871..47802871hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643464
Samples
Known GenesPCNT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107827
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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