A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568769



Internal ID20941840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14375410..14376693hg38UCSC Ensembl
chr9:14375409..14376692hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381284
hg191284
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280183
Samples
Known GenesNFIB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568769
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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