A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067469



Internal ID21976702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95125844..95125844hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067469
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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