A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624444



Internal ID21572749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107944839..107944839hg38UCSC Ensembl
chr4:108865995..108865995hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123898
SamplesHG03125
Known GenesCYP2U1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624444
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