A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199989



Internal ID22349502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1602897..1602950hg38UCSC Ensembl
chr20:1583543..1583596hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14421564
SamplesHG00514
Known GenesSIRPB1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199989
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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