A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649396



Internal ID21597701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70949111..70949111hg38UCSC Ensembl
chr14:71415828..71415828hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081606
SamplesHG00732
Known GenesPCNX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649396
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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