A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416038



Internal ID21073591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5025201..5118600hg38UCSC Ensembl
chr9:5025201..5118600hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3893400
hg1993400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217461
Samples
Known GenesJAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416038
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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