A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439888



Internal ID21097441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99814301..99821900hg38UCSC Ensembl
chr9:102576583..102584182hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221665
Samples
Known GenesNR4A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439888
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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