A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176483



Internal ID22333900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152972828..152972913hg38UCSC Ensembl
chr6:153293963..153294048hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14455910
SamplesHG00733
Known GenesFBXO5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176483
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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