A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291029



Internal ID20500247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47684710..47684710hg38UCSC Ensembl
chr18:45211081..45211081hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765285
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291029
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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