A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567090



Internal ID20940161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85950984..85951784hg38UCSC Ensembl
chr9:88565899..88566699hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281289
Samples
Known GenesNAA35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567090
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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