A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633042



Internal ID21581347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124670520..124670520hg38UCSC Ensembl
chr9:127432799..127432799hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160063
SamplesHG03125
Known GenesMIR181A2HG, NR6A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633042
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