A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201483



Internal ID22350785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75540258..75552793hg38UCSC Ensembl
chr13:76114394..76126929hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3812536
hg1912536
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380173
SamplesNA19240
Known GenesUCHL3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201483
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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