A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294951



Internal ID20504169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86899324..86899454hg38UCSC Ensembl
chr1:87365007..87365137hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743761
Supporting Variants
Samples
Known GenesSEP15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294951
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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