A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269458



Internal ID20478676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29667172..29667172hg38UCSC Ensembl
chr8:29524688..29524688hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758493
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269458
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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