A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568367



Internal ID20941438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125226867..125227519hg38UCSC Ensembl
chr9:127989146..127989798hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279876
Samples
Known GenesRABEPK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568367
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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