A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282645



Internal ID20491863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183449690..183449690hg38UCSC Ensembl
chr3:183167478..183167478hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758413
Supporting Variants
Samples
Known GenesLINC00888
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282645
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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