A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066906



Internal ID21976139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139772869..139772869hg38UCSC Ensembl
chr3:139491711..139491711hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540537
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066906
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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