A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730061



Internal ID21400877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63058456..63264087hg38UCSC Ensembl
chr9:66963428..67219059hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38205632
hg19255632
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256094
SamplesNA19238
Known GenesLOC286297
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730061
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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