A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258061



Internal ID21398180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87913699..88141469hg38UCSC Ensembl
chr9:90528614..90756384hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38227771
hg19227771
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730237
Supporting Variants
SamplesHG00513
Known GenesCDK20, SPATA31C1, SPATA31C2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258061
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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