A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201968



Internal ID22351195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69241042..69241528hg38UCSC Ensembl
chr13:69815174..69815660hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14443094
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201968
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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