A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671299



Internal ID21619604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:16264214..16321104hg38UCSC Ensembl
chrY:18376094..18432984hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3856891
hg1956891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169273
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671299
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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