A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559186



Internal ID20932257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125130675..125131234hg38UCSC Ensembl
chr9:127892954..127893513hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279862
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559186
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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