A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562052



Internal ID20935123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13856652..13860858hg38UCSC Ensembl
chr9:13856651..13860857hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384207
hg194207
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562052
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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