A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666991



Internal ID21615297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233409..40235417hg38UCSC Ensembl
chr4:40235029..40237037hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382009
hg192009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120406
SamplesHG00731
Known GenesRHOH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666991
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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