A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657739



Internal ID21606044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24212555..24212555hg38UCSC Ensembl
chr14:24681761..24681761hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080499
SamplesHG00731
Known GenesCHMP4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657739
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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