A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282547



Internal ID20491765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67819066..67819123hg38UCSC Ensembl
chr15:68111404..68111461hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739258
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282547
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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