A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568727



Internal ID20941798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135458657..135516088hg38UCSC Ensembl
chr9:138350503..138407934hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3857432
hg1957432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280146
Samples
Known GenesC9orf116, MRPS2, PPP1R26, PPP1R26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568727
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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