A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089222



Internal ID21508512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53220603..53220603hg38UCSC Ensembl
chr13:53794738..53794738hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646671
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089222
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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