A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418737



Internal ID21076290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5058901..5060100hg38UCSC Ensembl
chr9:5058901..5060100hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190912
Samples
Known GenesJAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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