A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117519



Internal ID21472408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60087689..60087689hg38UCSC Ensembl
chr20:58662744..58662744hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672428
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117519
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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