A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054428



Internal ID21963661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158218698..158218698hg38UCSC Ensembl
chr1:158188488..158188488hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382224
hg192224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054428
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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