A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563783



Internal ID20936854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116269279..116273197hg38UCSC Ensembl
chr9:119031558..119035476hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383919
hg193919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279683
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563783
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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