A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117550



Internal ID21475311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6070625..6070625hg38UCSC Ensembl
chr20:6051271..6051271hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656605
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117550
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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