A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619761



Internal ID21568066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100037436..100037436hg38UCSC Ensembl
chr2:100653898..100653898hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107406
SamplesNA19239
Known GenesAFF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619761
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