A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562896



Internal ID20935967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80879420..80880274hg38UCSC Ensembl
chr9:83494335..83495189hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562896
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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