A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7856n152



Internal ID22823559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35789939..35802531hg38UCSC Ensembl
chr6:35757716..35770308hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3812593
hg1912593
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3178297, nsv3179484
SamplesNA19240, HG00514
Known GenesCLPS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv7856n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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