A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066990



Internal ID21976223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139076813..139076813hg38UCSC Ensembl
chr6:139397950..139397950hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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