A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv787n152



Internal ID22816490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9364768..9367018hg38UCSC Ensembl
chr10:9406731..9408981hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382251
hg192251
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3208609, nsv3196064
SamplesNA19240, HG00733, 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)dgv787n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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