A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278153



Internal ID20487371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28728719..28728786hg38UCSC Ensembl
chr1:29055231..29055298hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278153
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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