A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018698



Internal ID21928041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47146799..47152982hg38UCSC Ensembl
chr6:47114535..47120718hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg386184
hg196184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018698
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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