A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566992



Internal ID20940063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112460271..112464234hg38UCSC Ensembl
chr9:115222551..115226514hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383964
hg193964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279603
Samples
Known GenesHSDL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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