A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664074



Internal ID21612379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64822372..64822372hg38UCSC Ensembl
chr14:65289090..65289090hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095294
SamplesHG00731
Known GenesSPTB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664074
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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