A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560845



Internal ID20933916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128976972..128977344hg38UCSC Ensembl
chr9:131739251..131739623hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280005
Samples
Known GenesNUP188
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560845
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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