A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7785n152



Internal ID22823488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24683759..24684456hg38UCSC Ensembl
chr6:24683987..24684684hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3176532, nsv3183189
SamplesNA19240, HG00733, HG00514
Known GenesACOT13
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv7785n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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