A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663882



Internal ID21612187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102239420..102239420hg38UCSC Ensembl
chr14:102705757..102705757hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080036
SamplesNA12878
Known GenesMOK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663882
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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