A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2214n152



Internal ID22817917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31066564..31067726hg38UCSC Ensembl
chr13:31640701..31641863hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381163
hg191163
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3204464, nsv3194890
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2214n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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