A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269073



Internal ID20478291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143182126..143182126hg38UCSC Ensembl
chr8:144263543..144263543hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755078
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269073
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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