A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763666



Internal ID20539526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70211317..70211317hg38UCSC Ensembl
chr18:67878553..67878553hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763666
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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