A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766138



Internal ID20541998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5006494..5006494hg38UCSC Ensembl
chr9:5006494..5006494hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277924
Samples
Known GenesJAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766138
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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