A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013646



Internal ID21922989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18321817..18331302hg38UCSC Ensembl
chr6:18322048..18331533hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg389486
hg199486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013646
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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