A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664395



Internal ID21612700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25112545..25112545hg38UCSC Ensembl
chr14:25581751..25581751hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099437
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664395
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer