A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276811



Internal ID20486029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33052370..33052370hg38UCSC Ensembl
chr1:33517971..33517971hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763277
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276811
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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