A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190372



Internal ID22341246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66146710..66147938hg38UCSC Ensembl
chr13:66720842..66722070hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2314n152
Supporting Variantsnssv14416950
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)nsv3190372
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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