A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047521



Internal ID21956754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143247958..143247958hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047521
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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