A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016555



Internal ID21925898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26507457..26507536hg38UCSC Ensembl
chr8:26364973..26365052hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559831
Samples
Known GenesPNMA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016555
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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