A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101352



Internal ID21508816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59410554..59410554hg38UCSC Ensembl
chr18:57077786..57077786hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645224
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101352
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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