A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067770



Internal ID21977003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39469438..39469438hg38UCSC Ensembl
chr3:39510929..39510929hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553828
Samples
Known GenesMOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067770
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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