A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14378345



Internal ID22324821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166858895..166858956hg38UCSC Ensembl
chr6:167272383..167272444hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3180902
Supporting Variants
SamplesNA19240
Known GenesRPS6KA2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14378345
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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