A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798416



Internal ID21243755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25033666..25033666hg38UCSC Ensembl
chr18:22613630..22613630hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13686399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798416
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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