A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751659



Internal ID20527519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11509268..11509268hg38UCSC Ensembl
chr18:11509267..11509267hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751659
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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