A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109257



Internal ID22018490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233407..40235439hg38UCSC Ensembl
chr4:40235027..40237059hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382033
hg192033
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550680
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109257
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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