A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200295



Internal ID22349768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66129156..66144586hg38UCSC Ensembl
chr9:42376680..42392106hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3815431
hg1915427
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439748
SamplesHG00514
Known GenesANKRD20A2, ANKRD20A3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200295
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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