A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665004



Internal ID21613309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15742645..15760586hg38UCSC Ensembl
chr10:15784644..15802585hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817942
hg1917942
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069262
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665004
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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