A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284046



Internal ID20493264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89994428..89994428hg38UCSC Ensembl
chr8:91006656..91006656hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768117
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284046
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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