A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618300



Internal ID21566605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1360820..1360820hg38UCSC Ensembl
chrY:1429713..1429713hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381046
hg191046
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169811
SamplesHG03732
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618300
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