A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567833



Internal ID20940904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124245684..124246123hg38UCSC Ensembl
chr9:127007963..127008402hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567833
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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