A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17102049



Internal ID21471589
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 StatusS
Merged Variantsnsv5650656
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17102049
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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