A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188215



Internal ID22340139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997795..166998780hg38UCSC Ensembl
chr6:167411283..167412268hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14400538
SamplesNA19240
Known GenesMIR3939
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3188215
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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