A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568951



Internal ID20942022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94253416..94257886hg38UCSC Ensembl
chr9:97015698..97020168hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384471
hg194471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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