A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115159



Internal ID21495532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1150048..1150048hg38UCSC Ensembl
chr20:1130691..1130691hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381550
hg191550
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661861
Supporting Variants
SamplesNA19238
Known GenesPSMF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115159
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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