A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567241



Internal ID20940312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113264667..113265543hg38UCSC Ensembl
chr9:116026947..116027823hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7916n223
Supporting Variantsnssv18279640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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