A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645402



Internal ID21593707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81252880..81252880hg38UCSC Ensembl
chr14:81719224..81719224hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg382754
hg192754
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092027
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645402
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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