A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257923



Internal ID21398246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87918874..88139672hg38UCSC Ensembl
chr9:90533789..90754587hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38220799
hg19220799
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)nssv16257923
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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