A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858137



Internal ID22633072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5059302..5060601hg38UCSC Ensembl
chr9:5059302..5060601hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513673
Samples
Known GenesJAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858137
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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