A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562677



Internal ID20935748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112770326..112770794hg38UCSC Ensembl
chr9:115532606..115533074hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279624
Samples
Known GenesSNX30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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