A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289870



Internal ID20499088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152972824..152972909hg38UCSC Ensembl
chr6:153293959..153294044hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740401
Supporting Variants
Samples
Known GenesFBXO5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289870
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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