A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259393



Internal ID20468611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166677458..166677458hg38UCSC Ensembl
chr1:166646695..166646695hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259393
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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