A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671980



Internal ID21620092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57350906..57350906hg38UCSC Ensembl
chr20:55925962..55925962hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116635
SamplesNA19238
Known GenesMIR5095
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671980
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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