A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042494



Internal ID21951810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225447234..225447234hg38UCSC Ensembl
chr1:225634936..225634936hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042494
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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