A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060836



Internal ID21970069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26335326..26335326hg38UCSC Ensembl
chr6:26335554..26335554hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060836
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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