A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671848



Internal ID21619960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41834738..41857144hg38UCSC Ensembl
chr15:42126936..42149342hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3822407
hg1922407
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095004
SamplesNA19239
Known GenesJMJD7, JMJD7-PLA2G4B, PLA2G4B, SPTBN5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671848
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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