A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565223



Internal ID20938294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88518227..88520139hg38UCSC Ensembl
chr9:91133142..91135054hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381913
hg191913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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