A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116498



Internal ID21468187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22561914..22561914hg38UCSC Ensembl
chr20:22542552..22542552hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667509
Supporting Variants
SamplesHG03125
Known GenesLINC00261
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116498
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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