A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655826



Internal ID21604131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10627190..10627190hg38UCSC Ensembl
chr18:10627187..10627187hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg386041
hg196041
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100116
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655826
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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