A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101370



Internal ID21401142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59968144..59968144hg38UCSC Ensembl
chr18:57635376..57635376hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663595
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101370
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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