A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625255



Internal ID21573560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6031446..6031446hg38UCSC Ensembl
chr10:6073409..6073409hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071206
SamplesHG00732
Known GenesIL2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625255
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