A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3247486



Internal ID22376730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13918760..13919716hg38UCSC Ensembl
chr18:13918759..13919715hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14290362
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3247486
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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