A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658401



Internal ID21606706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29452807..29452807hg38UCSC Ensembl
chr14:29922013..29922013hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086641
SamplesHG00171
Known GenesMIR548AI
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658401
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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