A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116803



Internal ID21458693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50367934..50367934hg38UCSC Ensembl
chr20:48984471..48984471hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665635
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116803
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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