A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066290



Internal ID21975523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16858243..16858243hg38UCSC Ensembl
chr6:16858474..16858474hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066290
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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