A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086822



Internal ID21996055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108982839..108982839hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3859
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086822
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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