A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565934



Internal ID20939005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113264593..113265631hg38UCSC Ensembl
chr9:116026873..116027911hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7916n223
Supporting Variantsnssv18279639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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