A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080386



Internal ID21989619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29460800..29460800hg38UCSC Ensembl
chr6:29428577..29428577hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576997
Samples
Known GenesOR2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080386
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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