A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647455



Internal ID21595760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23280704..23280704hg38UCSC Ensembl
chr14:23749913..23749913hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080439
SamplesHG00731
Known GenesHOMEZ
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647455
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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