A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14401103



Internal ID22290573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28176184..28178219hg38UCSC Ensembl
chr6:28143962..28145997hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg382036
hg192036
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186944
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14401103
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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