A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040585



Internal ID21949928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226811218..226811218hg38UCSC Ensembl
chr1:226998919..226998919hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040585
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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