A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14400538



Internal ID22328691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997795..166998780hg38UCSC Ensembl
chr6:167411283..167412268hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188215
Supporting Variants
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)nssv14400538
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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