A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669729



Internal ID21618034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40333147..40369327hg38UCSC Ensembl
chr15:40625348..40661528hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3836181
hg1936181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092095
SamplesNA19239
Known GenesC15orf52, DISP2, PHGR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669729
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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