A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569028



Internal ID20942099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32477747..32478321hg38UCSC Ensembl
chr9:32477745..32478319hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280483
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569028
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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