A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565535



Internal ID20938606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10618459..10618796hg38UCSC Ensembl
chr9:10618459..10618796hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565535
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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