A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203373



Internal ID22352397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34766956..34767368hg38UCSC Ensembl
chr13:35341093..35341505hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14416259
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203373
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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