A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200301



Internal ID22349773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33990041..33990527hg38UCSC Ensembl
chr19:34480946..34481432hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14420474
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)nsv3200301
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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