A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015164



Internal ID21924507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18026384..18026515hg38UCSC Ensembl
chr8:17883893..17884024hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558603
Samples
Known GenesPCM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015164
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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