A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051364



Internal ID21960598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224801748..224801748hg38UCSC Ensembl
chr1:224989450..224989450hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051364
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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