A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560740



Internal ID20933811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132962217..132963080hg38UCSC Ensembl
chr9:135837604..135838467hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38864
hg19864
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560740
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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