A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650656



Internal ID21598961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70211314..70211314hg38UCSC Ensembl
chr18:67878550..67878550hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17102049
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650656
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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