A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049827



Internal ID21959060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121963440..121963440hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049827
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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