A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061065



Internal ID21970298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168458351..168458351hg38UCSC Ensembl
chr6:168859031..168859031hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573871
Samples
Known GenesSMOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061065
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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