A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559812



Internal ID20932883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10964354..10966975hg38UCSC Ensembl
chr9:10964354..10966975hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg382622
hg192622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7567n223
Supporting Variantsnssv18279502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559812
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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