A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116028



Internal ID21422516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1259650..1259650hg38UCSC Ensembl
chr20:1240294..1240294hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656483
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116028
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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