A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117936



Internal ID21495999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62666118..62666118hg38UCSC Ensembl
chr20:61297470..61297470hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665446
Supporting Variants
SamplesNA19238
Known GenesLOC100127888, SLCO4A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117936
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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