A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282030



Internal ID20491248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159096298..159098492hg38UCSC Ensembl
chr1:159066088..159068282hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382195
hg192195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282030
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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