A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665446



Internal ID21613751
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 StatusM
Merged Variants
Supporting Variantsnssv17117936
SamplesNA19238
Known GenesLOC100127888, SLCO4A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665446
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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