A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763415



Internal ID20539275
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 StatusM
Merged Variants
Supporting Variantsnssv16259393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763415
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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