A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666077



Internal ID21614382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18568182..18776762hg38UCSC Ensembl
chr17:18471496..18680075hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38208581
hg19208580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092583
SamplesNA19239
Known GenesCCDC144B, FBXW10, FOXO3B, TBC1D28, TRIM16L, ZNF286B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666077
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer