A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055025



Internal ID21964258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22575417..22575417hg38UCSC Ensembl
chr1:22901910..22901910hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528933
Samples
Known GenesEPHA8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055025
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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