A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568168



Internal ID20941239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93784711..93784833hg38UCSC Ensembl
chr9:96546993..96547115hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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