A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052364



Internal ID21961598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143247916..143247916hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052364
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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