A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284887



Internal ID20494105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33462145..33462145hg38UCSC Ensembl
chr8:33319663..33319663hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763494
Supporting Variants
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284887
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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