A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730237



Internal ID21401048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87868106..88141469hg38UCSC Ensembl
chr9:90483021..90756384hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38273364
hg19273364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258061, nssv16256478, nssv16257923, nssv16256234
SamplesHG00513
Known GenesCDK20, SPATA31C1, SPATA31C2, SPATA31E1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730237
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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