A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570569



Internal ID20943640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112460462..112461378hg38UCSC Ensembl
chr9:115222742..115223658hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279604
Samples
Known GenesHSDL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570569
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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