A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7750n152



Internal ID22823453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13925069..13925267hg38UCSC Ensembl
chr6:13925300..13925498hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3184380, nsv3189564, nsv3171602
SamplesNA19240, HG00733, HG00514
Known GenesRNF182
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv7750n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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