A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559766



Internal ID20932837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4621675..4623068hg38UCSC Ensembl
chr9:4621675..4623068hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280733
Samples
Known GenesSPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559766
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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