A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105464



Internal ID22014697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14842121..14842121hg38UCSC Ensembl
chr21:16214442..16214442hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105464
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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