A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188980



Internal ID22340535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5835666..5835947hg38UCSC Ensembl
chr6:5835899..5836180hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14411012, nssv14436519, nssv14453175
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)nsv3188980
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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