A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569191



Internal ID20942262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109034717..109034946hg38UCSC Ensembl
chr9:111796997..111797226hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279480
Samples
Known GenesTMEM245
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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