A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566838



Internal ID20939909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120673894..120674660hg38UCSC Ensembl
chr9:123436172..123436938hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279733
Samples
Known GenesMEGF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566838
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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