A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653855



Internal ID21602160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48112909..48112909hg38UCSC Ensembl
chr14:48582112..48582112hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094228
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653855
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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