A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655359



Internal ID21603664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10414492..10414492hg38UCSC Ensembl
chr18:10414489..10414489hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100108
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655359
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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