A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066466



Internal ID21975699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106111520..106111520hg38UCSC Ensembl
chr3:105830367..105830367hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066466
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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