A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765401



Internal ID20541261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11489185..11489185hg38UCSC Ensembl
chr18:11489184..11489184hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765401
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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