A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389048



Internal ID21380183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84888972..84889290hg38UCSC Ensembl
chr9:87503887..87504205hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704678
Samples
Known GenesNTRK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389048
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer