A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206267



Internal ID22354833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10269566..10269741hg38UCSC Ensembl
chr20:10250214..10250389hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14394709
SamplesNA19240
Known GenesSNAP25
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206267
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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