A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061160



Internal ID21970393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121651136..121651136hg38UCSC Ensembl
chr8:122663376..122663376hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061160
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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