A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197492



Internal ID22347366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9603210..9606282hg38UCSC Ensembl
chr18:9603208..9606280hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383073
hg193073
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3761n152
Supporting Variantsnssv14446966
SamplesHG00733
Known GenesPPP4R1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197492
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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