A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264710



Internal ID20473928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220971692..220971692hg38UCSC Ensembl
chr1:221145034..221145034hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264710
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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